Canonical Allele Identifier: CA534167390
Gene: VAMP5 HGNC NCBI

Linked Data

dbSNP Id: rs1025562999
gnomAD v2: 2-85816405-C-T
gnomAD v3: 2-85589282-C-T
gnomAD v4: 2-85589282-C-T
MyVariant Identifiers: chr2:g.85816405C>T (hg19) chr2:g.85589282C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85589282C>T , CM000664.2:g.85589282C>T GRCh38
NC_000002.11:g.85816405C>T , CM000664.1:g.85816405C>T GRCh37
NC_000002.10:g.85669916C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306384.5:c.4-2443C>T MANE Select ENSP00000305647.4:n.4-2443C>T
ENST00000306384.4:c.4-2443C>T ENSP00000305647.4:n.4-2443C>T
NM_006634.2:c.4-2443C>T NP_006625.1:n.4-2443C>T
NM_006634.3:c.4-2443C>T MANE Select NP_006625.1:n.4-2443C>T
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