Canonical Allele Identifier: CA534167387
Gene: VAMP5 HGNC NCBI

Linked Data

dbSNP Id: rs1200257547
gnomAD v2: 2-85816390-C-A
gnomAD v3: 2-85589267-C-A
gnomAD v4: 2-85589267-C-A
MyVariant Identifiers: chr2:g.85816390C>A (hg19) chr2:g.85589267C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85589267C>A , CM000664.2:g.85589267C>A GRCh38
NC_000002.11:g.85816390C>A , CM000664.1:g.85816390C>A GRCh37
NC_000002.10:g.85669901C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306384.5:c.4-2458C>A MANE Select ENSP00000305647.4:n.4-2458C>A
ENST00000306384.4:c.4-2458C>A ENSP00000305647.4:n.4-2458C>A
NM_006634.2:c.4-2458C>A NP_006625.1:n.4-2458C>A
NM_006634.3:c.4-2458C>A MANE Select NP_006625.1:n.4-2458C>A
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