Canonical Allele Identifier: CA2221132771
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108564T= , CM000678.2:g.49108564T= GRCh38
NC_000016.9:g.49142475T= , CM000678.1:g.49142475T= GRCh37
NC_000016.8:g.47699976T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933517.1:n.810+1380A=
XR_001752138.2:n.591+5412A=
XR_933517.2:n.810+1380A=