Canonical Allele Identifier: CA467132465
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

dbSNP Id: rs1196115739
gnomAD v3: 9-125241709-G-C
gnomAD v4: 9-125241709-G-C
MyVariant Identifiers: chr9:g.128003988G>C (hg19) chr9:g.125241709G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241709G>C , CM000671.2:g.125241709G>C GRCh38
NC_000009.11:g.128003988G>C , CM000671.1:g.128003988G>C GRCh37
NC_000009.10:g.127043809G>C NCBI36
NG_027761.1:g.4679C>G

Transcript Alleles

HGVS Amino-acid change
XM_011518501.1:c.-696G>C (GAPVD1) XP_011516803.1:n.-696G>C
XM_011518503.1:c.-1002G>C (GAPVD1) XP_011516805.1:n.-1002G>C
XM_011518504.1:c.-647G>C (GAPVD1) XP_011516806.1:n.-647G>C
XR_001746927.1:n.47G>C (HSPA5-DT)
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