Canonical Allele Identifier: CA2221132884
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108796A= , CM000678.2:g.49108796A= GRCh38
NC_000016.9:g.49142707A= , CM000678.1:g.49142707A= GRCh37
NC_000016.8:g.47700208A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933517.1:n.810+1148T=
XR_001752138.2:n.591+5180T=
XR_933517.2:n.810+1148T=