Canonical Allele Identifier: CA1356976018

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.35101019G= , CM000665.2:g.35101019G=	GRCh38
NC_000003.11:g.35142511G= , CM000665.1:g.35142511G=	GRCh37
NC_000003.10:g.35117515G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110817.1:n.206+205452C=