Canonical Allele Identifier: CA467132629
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

gnomAD v4: 9-125241756-G-A
MyVariant Identifiers: chr9:g.128004035G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241756G>A , CM000671.2:g.125241756G>A GRCh38
NC_000009.11:g.128004035G>A , CM000671.1:g.128004035G>A GRCh37
NC_000009.10:g.127043856G>A NCBI36
NG_027761.1:g.4632C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011518501.1:c.-649G>A (GAPVD1) XP_011516803.1:n.-649G>A
XM_011518503.1:c.-955G>A (GAPVD1) XP_011516805.1:n.-955G>A
XM_011518504.1:c.-600G>A (GAPVD1) XP_011516806.1:n.-600G>A
XR_001746927.1:n.94G>A (HSPA5-DT)
Search 100 bp 5'
Search 100 bp 3'