Canonical Allele Identifier: CA2355978787
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661831T= , CM000682.2:g.23661831T= GRCh38
NC_000020.10:g.23642468T= , CM000682.1:g.23642468T= GRCh37
NC_000020.9:g.23590468T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+181T=