Canonical Allele Identifier: CA2839699668

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.69755851A>T , CM000677.2:g.69755851A>T	GRCh38
NC_000015.9:g.70048190A>T , CM000677.1:g.70048190A>T	GRCh37
NC_000015.8:g.67835244A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001751592.2:n.86-305A>T