Canonical Allele Identifier: CA287514002
Gene: VAMP2 HGNC NCBI

Linked Data

dbSNP Id: rs761425233
MyVariant Identifiers: chr17:g.8159183C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8159183C>G , CM000679.2:g.8159183C>G GRCh38
NC_000017.10:g.8062501C>G , CM000679.1:g.8062501C>G GRCh37
NC_000017.9:g.8003226C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000316509.11:c.*1672G>C MANE Select ENSP00000314214.6:n.*1672G>C
ENST00000316509.10:c.*1672G>C ENSP00000314214.6:n.*1672G>C
ENST00000498285.1:c.334+2290G>C ENSP00000464383.1:n.334+2290G>C
NM_014232.2:c.*1672G>C NP_055047.2:n.*1672G>C
NM_001330125.1:c.*1672G>C NP_001317054.1:n.*1672G>C
NM_014232.3:c.*1672G>C MANE Select NP_055047.2:n.*1672G>C