Canonical Allele Identifier: CA2221132896
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108849C= , CM000678.2:g.49108849C= GRCh38
NC_000016.9:g.49142760C= , CM000678.1:g.49142760C= GRCh37
NC_000016.8:g.47700261C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933517.1:n.810+1095G=
XR_001752138.2:n.591+5127G=
XR_933517.2:n.810+1095G=