Allele/Variant

rs762532614

Species
Homo sapiens
Symbol
rs762532614
Category
Variant
Variant type
SNP
Overlaps
AP2S1
Location
19:46838513
Nucleotide Change
G>A
Most Severe Consequence
  • synonymous variant
See all consequences
HGVS.g name
  • NC_000019.10:g.46838513G>A
HGVS.c name
  • ENSEMBL:ENST00000263270.11:c.363C>T
  • ENSEMBL:ENST00000352203.8:c.405C>T
HGVS.p name
  • ENSP00000263270:p.Gly121=
  • ENSP00000263271:p.Gly135=
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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