Canonical Allele Identifier: CA2298481276

Gene:

Linked Data

• dbSNP Id: rs2848745

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.41477761G>T , CM000680.2:g.41477761G>T	GRCh38
NC_000018.9:g.39057725G>T , CM000680.1:g.39057725G>T	GRCh37
NC_000018.8:g.37311723G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935409.1:n.86-26373G>T