Canonical Allele Identifier: CA1502658789

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148731458C= , CM000666.2:g.148731458C=	GRCh38
NC_000004.11:g.149652610C= , CM000666.1:g.149652610C=	GRCh37
NC_000004.10:g.149872060C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001741441.1:n.1746-135299C=