Canonical Allele Identifier: CA2221132887
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108814C= , CM000678.2:g.49108814C= GRCh38
NC_000016.9:g.49142725C= , CM000678.1:g.49142725C= GRCh37
NC_000016.8:g.47700226C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933517.1:n.810+1130G=
XR_001752138.2:n.591+5162G=
XR_933517.2:n.810+1130G=