Canonical Allele Identifier: CA2779324553

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20734949G>T , CM000670.2:g.20734949G>T	GRCh38
NC_000008.10:g.20592460G>T , CM000670.1:g.20592460G>T	GRCh37
NC_000008.9:g.20636740G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_949569.3:n.72-55497G>T