Canonical Allele Identifier: CA1889344582
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697719C= , CM000672.2:g.8697719C= GRCh38
NC_000010.10:g.8739682C= , CM000672.1:g.8739682C= GRCh37
NC_000010.9:g.8779688C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27918G=