Canonical Allele Identifier: CA467132794
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

dbSNP Id: rs1588432621
MyVariant Identifiers: chr9:g.128004088T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241809T>C , CM000671.2:g.125241809T>C GRCh38
NC_000009.11:g.128004088T>C , CM000671.1:g.128004088T>C GRCh37
NC_000009.10:g.127043909T>C NCBI36
NG_027761.1:g.4579A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011518501.1:c.-596T>C (GAPVD1) XP_011516803.1:n.-596T>C
XM_011518503.1:c.-902T>C (GAPVD1) XP_011516805.1:n.-902T>C
XM_011518504.1:c.-547T>C (GAPVD1) XP_011516806.1:n.-547T>C
XR_001746927.1:n.147T>C (HSPA5-DT)
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