Canonical Allele Identifier: CA467132469
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.128003989A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241710A>C , CM000671.2:g.125241710A>C GRCh38
NC_000009.11:g.128003989A>C , CM000671.1:g.128003989A>C GRCh37
NC_000009.10:g.127043810A>C NCBI36
NG_027761.1:g.4678T>G

Transcript Alleles

HGVS Amino-acid change
XM_011518501.1:c.-695A>C (GAPVD1) XP_011516803.1:n.-695A>C
XM_011518503.1:c.-1001A>C (GAPVD1) XP_011516805.1:n.-1001A>C
XM_011518504.1:c.-646A>C (GAPVD1) XP_011516806.1:n.-646A>C
XR_001746927.1:n.48A>C (HSPA5-DT)