Canonical Allele Identifier: CA2246164891
Gene: VAMP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8159205T= , CM000679.2:g.8159205T= GRCh38
NC_000017.10:g.8062523T= , CM000679.1:g.8062523T= GRCh37
NC_000017.9:g.8003248T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000316509.11:c.*1650A= MANE Select ENSP00000314214.6:n.*1650A=
ENST00000316509.10:c.*1650A= ENSP00000314214.6:n.*1650A=
ENST00000498285.1:c.334+2268A= ENSP00000464383.1:n.334+2268A=
NM_014232.2:c.*1650A= NP_055047.2:n.*1650A=
NM_001330125.1:c.*1650A= NP_001317054.1:n.*1650A=
NM_014232.3:c.*1650A= MANE Select NP_055047.2:n.*1650A=
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