Canonical Allele Identifier: CA2221132902
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108864A= , CM000678.2:g.49108864A= GRCh38
NC_000016.9:g.49142775A= , CM000678.1:g.49142775A= GRCh37
NC_000016.8:g.47700276A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933517.1:n.810+1080T=
XR_001752138.2:n.591+5112T=
XR_933517.2:n.810+1080T=