Canonical Allele Identifier: CA2061106190

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.106556209G= , CM000674.2:g.106556209G=	GRCh38
NC_000012.11:g.106949987G= , CM000674.1:g.106949987G=	GRCh37
NC_000012.10:g.105474117G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040246.1:n.143-48399C=