Canonical Allele Identifier: CA981235182
Gene: VAMP2 HGNC NCBI

Linked Data

gnomAD v3: 17-8159235-A-C
gnomAD v4: 17-8159235-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8159235A>C , CM000679.2:g.8159235A>C GRCh38
NC_000017.10:g.8062553A>C , CM000679.1:g.8062553A>C GRCh37
NC_000017.9:g.8003278A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000316509.11:c.*1620T>G MANE Select ENSP00000314214.6:n.*1620T>G
ENST00000316509.10:c.*1620T>G ENSP00000314214.6:n.*1620T>G
ENST00000498285.1:c.334+2238T>G ENSP00000464383.1:n.334+2238T>G
NM_014232.2:c.*1620T>G NP_055047.2:n.*1620T>G
NM_001330125.1:c.*1620T>G NP_001317054.1:n.*1620T>G
NM_014232.3:c.*1620T>G MANE Select NP_055047.2:n.*1620T>G
Search 100 bp 5'
Search 100 bp 3'