Canonical Allele Identifier: CA2703023328

Gene:

Linked Data

• dbSNP Id: rs2106651873

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.72266726A>T , CM000665.2:g.72266726A>T	GRCh38
NC_000003.11:g.72315877A>T , CM000665.1:g.72315877A>T	GRCh37
NC_000003.10:g.72398567A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940958.1:n.835+8382T>A