Canonical Allele Identifier: CA1889344569
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697682A= , CM000672.2:g.8697682A= GRCh38
NC_000010.10:g.8739645A= , CM000672.1:g.8739645A= GRCh37
NC_000010.9:g.8779651A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.33-27881T=