Canonical Allele Identifier: CA2635972881
Gene: VAMP2 HGNC NCBI

Linked Data

gnomAD v4: 17-8159356-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8159356T>C , CM000679.2:g.8159356T>C GRCh38
NC_000017.10:g.8062674T>C , CM000679.1:g.8062674T>C GRCh37
NC_000017.9:g.8003399T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000316509.11:c.*1499A>G MANE Select ENSP00000314214.6:n.*1499A>G
ENST00000316509.10:c.*1499A>G ENSP00000314214.6:n.*1499A>G
ENST00000498285.1:c.334+2117A>G ENSP00000464383.1:n.334+2117A>G
NM_014232.2:c.*1499A>G NP_055047.2:n.*1499A>G
XM_005256775.3:c.*1499A>G XP_005256832.1:n.*1499A>G
NM_001330125.1:c.*1499A>G NP_001317054.1:n.*1499A>G
NM_014232.3:c.*1499A>G MANE Select NP_055047.2:n.*1499A>G
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