Canonical Allele Identifier: CA467132466
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.128003988G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241709G>T , CM000671.2:g.125241709G>T GRCh38
NC_000009.11:g.128003988G>T , CM000671.1:g.128003988G>T GRCh37
NC_000009.10:g.127043809G>T NCBI36
NG_027761.1:g.4679C>A

Transcript Alleles

HGVS Amino-acid change
XM_011518501.1:c.-696G>T (GAPVD1) XP_011516803.1:n.-696G>T
XM_011518503.1:c.-1002G>T (GAPVD1) XP_011516805.1:n.-1002G>T
XM_011518504.1:c.-647G>T (GAPVD1) XP_011516806.1:n.-647G>T
XR_001746927.1:n.47G>T (HSPA5-DT)