Canonical Allele Identifier: CA2059316553

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102571551A= , CM000674.2:g.102571551A=	GRCh38
NC_000012.11:g.102965329A= , CM000674.1:g.102965329A=	GRCh37
NC_000012.10:g.101489459A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001749289.1:n.1952+87663A=