Canonical Allele Identifier: CA2815584529
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661865T>C , CM000682.2:g.23661865T>C GRCh38
NC_000020.10:g.23642502T>C , CM000682.1:g.23642502T>C GRCh37
NC_000020.9:g.23590502T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+215T>C