Allele/Variant

rs762864452

Species
Homo sapiens
Symbol
rs762864452
Category
Variant
Variant type
SNP
Overlaps
MMP9
Location
20:46012536
Nucleotide Change
G>C
Most Severe Consequence
  • synonymous variant
See all consequences
HGVS.g name
  • NC_000020.11:g.46012536G>C
HGVS.c name
  • ENSEMBL:ENST00000372330.3:c.1284G>C
  • RefSeq:NM_004994.3:c.1284G>C
HGVS.p name
  • ENSP00000361405:p.Gly428=
  • NP_004985:p.Gly428=
Synonyms
Not Available
Notes
Not Available
Cross references
Not Available
References
Not Available

Genome location
Assembly version
Not Available
Viewer Help
Data currently unavailable; sequence viewer under construction

Variant Molecular Consequences

Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
No records match query. Try removing filters.
Showing 0 - 0 of 0 rows
per page