Canonical Allele Identifier: CA1573933688

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113660993C= , CM000667.2:g.113660993C=	GRCh38
NC_000005.9:g.112996690C= , CM000667.1:g.112996690C=	GRCh37
NC_000005.8:g.113024589C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742841.1:n.59+27629C=