Canonical Allele Identifier: CA2221132856
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108734A= , CM000678.2:g.49108734A= GRCh38
NC_000016.9:g.49142645A= , CM000678.1:g.49142645A= GRCh37
NC_000016.8:g.47700146A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933517.1:n.810+1210T=
XR_001752138.2:n.591+5242T=
XR_933517.2:n.810+1210T=