Canonical Allele Identifier: CA1876571564

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120294359G= , CM000671.2:g.120294359G=	GRCh38
NC_000009.11:g.123056637G= , CM000671.1:g.123056637G=	GRCh37
NC_000009.10:g.122096458G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930310.1:n.363+64838C=