Canonical Allele Identifier: CA467132419
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.128003974A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241695A>C , CM000671.2:g.125241695A>C GRCh38
NC_000009.11:g.128003974A>C , CM000671.1:g.128003974A>C GRCh37
NC_000009.10:g.127043795A>C NCBI36
NG_027761.1:g.4693T>G

Transcript Alleles

HGVS Amino-acid Change
XM_011518501.1:c.-710A>C (GAPVD1) XP_011516803.1:n.-710A>C
XM_011518503.1:c.-1016A>C (GAPVD1) XP_011516805.1:n.-1016A>C
XM_011518504.1:c.-661A>C (GAPVD1) XP_011516806.1:n.-661A>C
XR_001746927.1:n.33A>C (HSPA5-DT)
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