Canonical Allele Identifier: CA467132743
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

dbSNP Id: rs1231715826
gnomAD v4: 9-125241792-G-A
MyVariant Identifiers: chr9:g.128004071G>A (hg19) chr9:g.125241792G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241792G>A , CM000671.2:g.125241792G>A GRCh38
NC_000009.11:g.128004071G>A , CM000671.1:g.128004071G>A GRCh37
NC_000009.10:g.127043892G>A NCBI36
NG_027761.1:g.4596C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011518501.1:c.-613G>A (GAPVD1) XP_011516803.1:n.-613G>A
XM_011518503.1:c.-919G>A (GAPVD1) XP_011516805.1:n.-919G>A
XM_011518504.1:c.-564G>A (GAPVD1) XP_011516806.1:n.-564G>A
XR_001746927.1:n.130G>A (HSPA5-DT)
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