Canonical Allele Identifier: CA2815584527
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661759C>T , CM000682.2:g.23661759C>T GRCh38
NC_000020.10:g.23642396C>T , CM000682.1:g.23642396C>T GRCh37
NC_000020.9:g.23590396C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754712.1:n.280+109C>T