Canonical Allele Identifier: CA467132481
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

dbSNP Id: rs1237210067
gnomAD v3: 9-125241713-G-A
gnomAD v4: 9-125241713-G-A
MyVariant Identifiers: chr9:g.128003992G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241713G>A , CM000671.2:g.125241713G>A GRCh38
NC_000009.11:g.128003992G>A , CM000671.1:g.128003992G>A GRCh37
NC_000009.10:g.127043813G>A NCBI36
NG_027761.1:g.4675C>T

Transcript Alleles

HGVS Amino-acid change
XM_011518501.1:c.-692G>A (GAPVD1) XP_011516803.1:n.-692G>A
XM_011518503.1:c.-998G>A (GAPVD1) XP_011516805.1:n.-998G>A
XM_011518504.1:c.-643G>A (GAPVD1) XP_011516806.1:n.-643G>A
XR_001746927.1:n.51G>A (HSPA5-DT)
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