Canonical Allele Identifier: CA467132486
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.128003994C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241715C>G , CM000671.2:g.125241715C>G GRCh38
NC_000009.11:g.128003994C>G , CM000671.1:g.128003994C>G GRCh37
NC_000009.10:g.127043815C>G NCBI36
NG_027761.1:g.4673G>C

Transcript Alleles

HGVS Amino-acid change
XM_011518501.1:c.-690C>G (GAPVD1) XP_011516803.1:n.-690C>G
XM_011518503.1:c.-996C>G (GAPVD1) XP_011516805.1:n.-996C>G
XM_011518504.1:c.-641C>G (GAPVD1) XP_011516806.1:n.-641C>G
XR_001746927.1:n.53C>G (HSPA5-DT)