Canonical Allele Identifier: CA1872408656

Gene:

Linked Data

• dbSNP Id: rs2098067332

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.111236656A>G , CM000671.2:g.111236656A>G	GRCh38
NC_000009.11:g.113998936A>G , CM000671.1:g.113998936A>G	GRCh37
NC_000009.10:g.113038757A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_930247.1:n.476+36157T>C
XR_930248.1:n.556+36157T>C
XR_930249.1:n.476+36157T>C
XR_001746893.1:n.476+36157T>C
XR_001746894.1:n.476+36157T>C
XR_930247.2:n.476+36157T>C