Canonical Allele Identifier: CA2659858864
Gene: VAMP8 HGNC NCBI

Linked Data

gnomAD v4: 2-85581877-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85581877G>A , CM000664.2:g.85581877G>A GRCh38
NC_000002.11:g.85809000G>A , CM000664.1:g.85809000G>A GRCh37
NC_000002.10:g.85662511G>A NCBI36
NG_022887.1:g.9387G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263864.10:c.*161G>A MANE Select ENSP00000263864.5:n.*161G>A
ENST00000263864.9:c.*161G>A ENSP00000263864.5:n.*161G>A
ENST00000409760.1:c.*297G>A ENSP00000387094.1:n.*297G>A
ENST00000432071.1:c.*161G>A ENSP00000407984.1:n.*161G>A
NM_003761.4:c.*161G>A NP_003752.2:n.*161G>A
XM_017005170.1:c.*297G>A XP_016860659.1:n.*297G>A
NM_003761.5:c.*161G>A MANE Select NP_003752.2:n.*161G>A
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