Canonical Allele Identifier: CA467132484
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.128003993A>T (hg19)

Genomic Alleles

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

Transcript Alleles

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