Canonical Allele Identifier: CA1797411913

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.81478401G= , CM000670.2:g.81478401G=	GRCh38
NC_000008.10:g.82390636G= , CM000670.1:g.82390636G=	GRCh37
NC_000008.9:g.82553191G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745980.1:n.514+16427G=