Canonical Allele Identifier: CA199746901
Gene: GAPVD1 HGNC NCBI
HSPA5-DT HGNC NCBI

Linked Data

dbSNP Id: rs769705734
gnomAD v2: 9-128003997-C-T
gnomAD v3: 9-125241718-C-T
gnomAD v4: 9-125241718-C-T
MyVariant Identifiers: chr9:g.128003997C>T (hg19) chr9:g.125241718C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.125241718C>T , CM000671.2:g.125241718C>T GRCh38
NC_000009.11:g.128003997C>T , CM000671.1:g.128003997C>T GRCh37
NC_000009.10:g.127043818C>T NCBI36
NG_027761.1:g.4670G>A

Transcript Alleles

HGVS Amino-acid change
XM_011518501.1:c.-687C>T (GAPVD1) XP_011516803.1:n.-687C>T
XM_011518503.1:c.-993C>T (GAPVD1) XP_011516805.1:n.-993C>T
XM_011518504.1:c.-638C>T (GAPVD1) XP_011516806.1:n.-638C>T
XR_001746927.1:n.56C>T (HSPA5-DT)
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