Canonical Allele Identifier: CA467132327
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.128003945C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241666C>G , CM000671.2:g.125241666C>G GRCh38
NC_000009.11:g.128003945C>G , CM000671.1:g.128003945C>G GRCh37
NC_000009.10:g.127043766C>G NCBI36
NG_027761.1:g.4722G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011518501.1:c.-739C>G (GAPVD1) XP_011516803.1:n.-739C>G
XM_011518503.1:c.-1045C>G (GAPVD1) XP_011516805.1:n.-1045C>G
XM_011518504.1:c.-690C>G (GAPVD1) XP_011516806.1:n.-690C>G
XR_001746927.1:n.4C>G (HSPA5-DT)
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