Canonical Allele Identifier: CA1121377260

Gene:

Linked Data

• dbSNP Id: rs1824909129
• gnomAD v3: 9-12108922-A-G
• gnomAD v4: 9-12108922-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.12108922A>G , CM000671.2:g.12108922A>G	GRCh38
NC_000009.11:g.12108922A>G , CM000671.1:g.12108922A>G	GRCh37
NC_000009.10:g.12098922A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929481.1:n.166+7899T>C
XR_929482.1:n.260+7899T>C
XR_929481.2:n.166+7899T>C
XR_929482.2:n.260+7899T>C