Canonical Allele Identifier: CA467132565
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

gnomAD v4: 9-125241738-A-C
MyVariant Identifiers: chr9:g.128004017A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241738A>C , CM000671.2:g.125241738A>C GRCh38
NC_000009.11:g.128004017A>C , CM000671.1:g.128004017A>C GRCh37
NC_000009.10:g.127043838A>C NCBI36
NG_027761.1:g.4650T>G

Transcript Alleles

HGVS Amino-acid Change
XM_011518501.1:c.-667A>C (GAPVD1) XP_011516803.1:n.-667A>C
XM_011518503.1:c.-973A>C (GAPVD1) XP_011516805.1:n.-973A>C
XM_011518504.1:c.-618A>C (GAPVD1) XP_011516806.1:n.-618A>C
XR_001746927.1:n.76A>C (HSPA5-DT)
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