Canonical Allele Identifier: CA1373743899
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577112T= , CM000665.2:g.70577112T= GRCh38
NC_000003.11:g.70626263T= , CM000665.1:g.70626263T= GRCh37
NC_000003.10:g.70708953T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940947.1:n.407-1159A=
XR_001740559.1:n.367-1159A=