Canonical Allele Identifier: CA199746851
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

dbSNP Id: rs964244334

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241714A>C , CM000671.2:g.125241714A>C GRCh38
NC_000009.11:g.128003993A>C , CM000671.1:g.128003993A>C GRCh37
NC_000009.10:g.127043814A>C NCBI36
NG_027761.1:g.4674T>G

Transcript Alleles

HGVS Amino-acid change
XM_011518501.1:c.-691A>C (GAPVD1) XP_011516803.1:n.-691A>C
XM_011518503.1:c.-997A>C (GAPVD1) XP_011516805.1:n.-997A>C
XM_011518504.1:c.-642A>C (GAPVD1) XP_011516806.1:n.-642A>C
XR_001746927.1:n.52A>C (HSPA5-DT)