Canonical Allele Identifier: CA1817441691

Gene:

Linked Data

• dbSNP Id: rs1812774624

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125478340C>T , CM000670.2:g.125478340C>T	GRCh38
NC_000008.10:g.126490582C>T , CM000670.1:g.126490582C>T	GRCh37
NC_000008.9:g.126559764C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+5026C>T