Canonical Allele Identifier: CA1889344486
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697499C= , CM000672.2:g.8697499C= GRCh38
NC_000010.10:g.8739462C= , CM000672.1:g.8739462C= GRCh37
NC_000010.9:g.8779468C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27698G=