Canonical Allele Identifier: CA467132722
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

dbSNP Id: rs1164152776
gnomAD v3: 9-125241784-C-T
gnomAD v4: 9-125241784-C-T
MyVariant Identifiers: chr9:g.128004063C>T (hg19) chr9:g.125241784C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241784C>T , CM000671.2:g.125241784C>T GRCh38
NC_000009.11:g.128004063C>T , CM000671.1:g.128004063C>T GRCh37
NC_000009.10:g.127043884C>T NCBI36
NG_027761.1:g.4604G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011518501.1:c.-621C>T (GAPVD1) XP_011516803.1:n.-621C>T
XM_011518503.1:c.-927C>T (GAPVD1) XP_011516805.1:n.-927C>T
XM_011518504.1:c.-572C>T (GAPVD1) XP_011516806.1:n.-572C>T
XR_001746927.1:n.122C>T (HSPA5-DT)
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