Canonical Allele Identifier: CA2221132785
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108595T= , CM000678.2:g.49108595T= GRCh38
NC_000016.9:g.49142506T= , CM000678.1:g.49142506T= GRCh37
NC_000016.8:g.47700007T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933517.1:n.810+1349A=
XR_001752138.2:n.591+5381A=
XR_933517.2:n.810+1349A=