Canonical Allele Identifier: CA2659858844
Gene: VAMP8 HGNC NCBI

Linked Data

gnomAD v4: 2-85581862-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85581862T>C , CM000664.2:g.85581862T>C GRCh38
NC_000002.11:g.85808985T>C , CM000664.1:g.85808985T>C GRCh37
NC_000002.10:g.85662496T>C NCBI36
NG_022887.1:g.9372T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263864.10:c.*146T>C MANE Select ENSP00000263864.5:n.*146T>C
ENST00000263864.9:c.*146T>C ENSP00000263864.5:n.*146T>C
ENST00000409760.1:c.*282T>C ENSP00000387094.1:n.*282T>C
ENST00000432071.1:c.*146T>C ENSP00000407984.1:n.*146T>C
NM_003761.4:c.*146T>C NP_003752.2:n.*146T>C
XM_017005170.1:c.*282T>C XP_016860659.1:n.*282T>C
NM_003761.5:c.*146T>C MANE Select NP_003752.2:n.*146T>C