Canonical Allele Identifier: CA2659858859
Gene: VAMP8 HGNC NCBI

Linked Data

gnomAD v4: 2-85581871-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85581871C>T , CM000664.2:g.85581871C>T GRCh38
NC_000002.11:g.85808994C>T , CM000664.1:g.85808994C>T GRCh37
NC_000002.10:g.85662505C>T NCBI36
NG_022887.1:g.9381C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263864.10:c.*155C>T MANE Select ENSP00000263864.5:n.*155C>T
ENST00000263864.9:c.*155C>T ENSP00000263864.5:n.*155C>T
ENST00000409760.1:c.*291C>T ENSP00000387094.1:n.*291C>T
ENST00000432071.1:c.*155C>T ENSP00000407984.1:n.*155C>T
NM_003761.4:c.*155C>T NP_003752.2:n.*155C>T
XM_017005170.1:c.*291C>T XP_016860659.1:n.*291C>T
NM_003761.5:c.*155C>T MANE Select NP_003752.2:n.*155C>T