Canonical Allele Identifier: CA467132702
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.128004056C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241777C>G , CM000671.2:g.125241777C>G GRCh38
NC_000009.11:g.128004056C>G , CM000671.1:g.128004056C>G GRCh37
NC_000009.10:g.127043877C>G NCBI36
NG_027761.1:g.4611G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011518501.1:c.-628C>G (GAPVD1) XP_011516803.1:n.-628C>G
XM_011518503.1:c.-934C>G (GAPVD1) XP_011516805.1:n.-934C>G
XM_011518504.1:c.-579C>G (GAPVD1) XP_011516806.1:n.-579C>G
XR_001746927.1:n.115C>G (HSPA5-DT)
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