Canonical Allele Identifier: CA467132496
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

dbSNP Id: rs953514059
MyVariant Identifiers: chr9:g.128003998C>T (hg19) chr9:g.125241719C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241719C>T , CM000671.2:g.125241719C>T GRCh38
NC_000009.11:g.128003998C>T , CM000671.1:g.128003998C>T GRCh37
NC_000009.10:g.127043819C>T NCBI36
NG_027761.1:g.4669G>A

Transcript Alleles

HGVS Amino-acid change
XM_011518501.1:c.-686C>T (GAPVD1) XP_011516803.1:n.-686C>T
XM_011518503.1:c.-992C>T (GAPVD1) XP_011516805.1:n.-992C>T
XM_011518504.1:c.-637C>T (GAPVD1) XP_011516806.1:n.-637C>T
XR_001746927.1:n.57C>T (HSPA5-DT)
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