Canonical Allele Identifier: CA467132483
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

dbSNP Id: rs964244334
gnomAD v3: 9-125241714-A-G
gnomAD v4: 9-125241714-A-G
MyVariant Identifiers: chr9:g.128003993A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241714A>G , CM000671.2:g.125241714A>G GRCh38
NC_000009.11:g.128003993A>G , CM000671.1:g.128003993A>G GRCh37
NC_000009.10:g.127043814A>G NCBI36
NG_027761.1:g.4674T>C

Transcript Alleles

HGVS Amino-acid change
XM_011518501.1:c.-691A>G (GAPVD1) XP_011516803.1:n.-691A>G
XM_011518503.1:c.-997A>G (GAPVD1) XP_011516805.1:n.-997A>G
XM_011518504.1:c.-642A>G (GAPVD1) XP_011516806.1:n.-642A>G
XR_001746927.1:n.52A>G (HSPA5-DT)
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