Canonical Allele Identifier: CA2355978768
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661788C= , CM000682.2:g.23661788C= GRCh38
NC_000020.10:g.23642425C= , CM000682.1:g.23642425C= GRCh37
NC_000020.9:g.23590425C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+138C=