Canonical Allele Identifier: CA1889344562
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697666A= , CM000672.2:g.8697666A= GRCh38
NC_000010.10:g.8739629A= , CM000672.1:g.8739629A= GRCh37
NC_000010.9:g.8779635A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27865T=