Canonical Allele Identifier: CA467132748
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.128004072G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241793G>C , CM000671.2:g.125241793G>C GRCh38
NC_000009.11:g.128004072G>C , CM000671.1:g.128004072G>C GRCh37
NC_000009.10:g.127043893G>C NCBI36
NG_027761.1:g.4595C>G

Transcript Alleles

HGVS Amino-acid Change
XM_011518501.1:c.-612G>C (GAPVD1) XP_011516803.1:n.-612G>C
XM_011518503.1:c.-918G>C (GAPVD1) XP_011516805.1:n.-918G>C
XM_011518504.1:c.-563G>C (GAPVD1) XP_011516806.1:n.-563G>C
XR_001746927.1:n.131G>C (HSPA5-DT)
Search 100 bp 5'
Search 100 bp 3'