Canonical Allele Identifier: CA2659858852
Gene: VAMP8 HGNC NCBI

Linked Data

gnomAD v4: 2-85581867-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85581867G>A , CM000664.2:g.85581867G>A GRCh38
NC_000002.11:g.85808990G>A , CM000664.1:g.85808990G>A GRCh37
NC_000002.10:g.85662501G>A NCBI36
NG_022887.1:g.9377G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263864.10:c.*151G>A MANE Select ENSP00000263864.5:n.*151G>A
ENST00000263864.9:c.*151G>A ENSP00000263864.5:n.*151G>A
ENST00000409760.1:c.*287G>A ENSP00000387094.1:n.*287G>A
ENST00000432071.1:c.*151G>A ENSP00000407984.1:n.*151G>A
NM_003761.4:c.*151G>A NP_003752.2:n.*151G>A
XM_017005170.1:c.*287G>A XP_016860659.1:n.*287G>A
NM_003761.5:c.*151G>A MANE Select NP_003752.2:n.*151G>A
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