Version: 8.0.0
Date: Tue Jan 28 2025
rs1370973378
Variant overlaps HLA-A
Homo sapiens
SummaryVariant Molecular Consequences
Allele/Variant

rs1370973378

Species
Homo sapiens
Symbol
rs1370973378
Category
Variant
Variant type
SNP
Overlaps
HLA-A
Location
6:29941373
Nucleotide Change
A>G
Most Severe Consequence
  • intron variant&non coding transcript variant
See all consequences
HGVS.g name
  • (GRCh38)6:29941373A>G
HGVS.c name
  • ENSEMBL:ENST00000396634.5:c.-282+54A>G
  • ENSEMBL:ENST00000849679.1:n.66-12827T>C
HGVS.p name
Not Available
Synonyms
Not Available
Notes
Not Available
Cross references
Not Available
References
Not Available
Genome location
Assembly version
Not Available
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Variant Molecular Consequences

Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
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