Canonical Allele Identifier: CA1702564126
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.41782351A= , CM000669.2:g.41782351A= GRCh38
NC_000007.13:g.41821949A= , CM000669.1:g.41821949A= GRCh37
NC_000007.12:g.41788474A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745185.1:n.964+46637A=
XR_001745186.1:n.954+46647A=