Canonical Allele Identifier: CA467132478
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

dbSNP Id: rs1237210067
gnomAD v3: 9-125241713-G-C
gnomAD v4: 9-125241713-G-C
MyVariant Identifiers: chr9:g.128003992G>C (hg19) chr9:g.125241713G>C (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
XM_011518501.1:c.-692G>C (GAPVD1) XP_011516803.1:n.-692G>C
XM_011518503.1:c.-998G>C (GAPVD1) XP_011516805.1:n.-998G>C
XM_011518504.1:c.-643G>C (GAPVD1) XP_011516806.1:n.-643G>C
XR_001746927.1:n.51G>C (HSPA5-DT)
Search 100 bp 5'
Search 100 bp 3'