Canonical Allele Identifier: CA51720455
Gene: VAMP5 HGNC NCBI

Linked Data

dbSNP Id: rs1011337127
MyVariant Identifiers: chr2:g.85816301A>G (hg19) chr2:g.85589178A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85589178A>G , CM000664.2:g.85589178A>G GRCh38
NC_000002.11:g.85816301A>G , CM000664.1:g.85816301A>G GRCh37
NC_000002.10:g.85669812A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306384.5:c.4-2547A>G MANE Select ENSP00000305647.4:n.4-2547A>G
ENST00000306384.4:c.4-2547A>G ENSP00000305647.4:n.4-2547A>G
NM_006634.2:c.4-2547A>G NP_006625.1:n.4-2547A>G
NM_006634.3:c.4-2547A>G MANE Select NP_006625.1:n.4-2547A>G
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