Canonical Allele Identifier: CA467132513
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.128004003G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241724G>A , CM000671.2:g.125241724G>A GRCh38
NC_000009.11:g.128004003G>A , CM000671.1:g.128004003G>A GRCh37
NC_000009.10:g.127043824G>A NCBI36
NG_027761.1:g.4664C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011518501.1:c.-681G>A (GAPVD1) XP_011516803.1:n.-681G>A
XM_011518503.1:c.-987G>A (GAPVD1) XP_011516805.1:n.-987G>A
XM_011518504.1:c.-632G>A (GAPVD1) XP_011516806.1:n.-632G>A
XR_001746927.1:n.62G>A (HSPA5-DT)