Canonical Allele Identifier: CA467132462
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.128003987G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241708G>C , CM000671.2:g.125241708G>C GRCh38
NC_000009.11:g.128003987G>C , CM000671.1:g.128003987G>C GRCh37
NC_000009.10:g.127043808G>C NCBI36
NG_027761.1:g.4680C>G

Transcript Alleles

HGVS Amino-acid change
XM_011518501.1:c.-697G>C (GAPVD1) XP_011516803.1:n.-697G>C
XM_011518503.1:c.-1003G>C (GAPVD1) XP_011516805.1:n.-1003G>C
XM_011518504.1:c.-648G>C (GAPVD1) XP_011516806.1:n.-648G>C
XR_001746927.1:n.46G>C (HSPA5-DT)