Canonical Allele Identifier: CA467132474
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

dbSNP Id: rs1474466408
MyVariant Identifiers: chr9:g.128003991T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241712T>C , CM000671.2:g.125241712T>C GRCh38
NC_000009.11:g.128003991T>C , CM000671.1:g.128003991T>C GRCh37
NC_000009.10:g.127043812T>C NCBI36
NG_027761.1:g.4676A>G

Transcript Alleles

HGVS Amino-acid change
XM_011518501.1:c.-693T>C (GAPVD1) XP_011516803.1:n.-693T>C
XM_011518503.1:c.-999T>C (GAPVD1) XP_011516805.1:n.-999T>C
XM_011518504.1:c.-644T>C (GAPVD1) XP_011516806.1:n.-644T>C
XR_001746927.1:n.50T>C (HSPA5-DT)