Canonical Allele Identifier: CA467132330
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.128003946G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241667G>C , CM000671.2:g.125241667G>C GRCh38
NC_000009.11:g.128003946G>C , CM000671.1:g.128003946G>C GRCh37
NC_000009.10:g.127043767G>C NCBI36
NG_027761.1:g.4721C>G

Transcript Alleles

HGVS Amino-acid Change
XM_011518501.1:c.-738G>C (GAPVD1) XP_011516803.1:n.-738G>C
XM_011518503.1:c.-1044G>C (GAPVD1) XP_011516805.1:n.-1044G>C
XM_011518504.1:c.-689G>C (GAPVD1) XP_011516806.1:n.-689G>C
XR_001746927.1:n.5G>C (HSPA5-DT)
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