Canonical Allele Identifier: CA199746955
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

dbSNP Id: rs978514680
MyVariant Identifiers: chr9:g.128004094C>T (hg19) chr9:g.125241815C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241815C>T , CM000671.2:g.125241815C>T GRCh38
NC_000009.11:g.128004094C>T , CM000671.1:g.128004094C>T GRCh37
NC_000009.10:g.127043915C>T NCBI36
NG_027761.1:g.4573G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011518501.1:c.-590C>T (GAPVD1) XP_011516803.1:n.-590C>T
XM_011518503.1:c.-896C>T (GAPVD1) XP_011516805.1:n.-896C>T
XM_011518504.1:c.-541C>T (GAPVD1) XP_011516806.1:n.-541C>T
XR_001746927.1:n.153C>T (HSPA5-DT)
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