Canonical Allele Identifier: CA1817441702

Gene:

Linked Data

• dbSNP Id: rs1812774726

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.125478345C>T , CM000670.2:g.125478345C>T	GRCh38
NC_000008.10:g.126490587C>T , CM000670.1:g.126490587C>T	GRCh37
NC_000008.9:g.126559769C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928628.1:n.256+5031C>T