Canonical Allele Identifier: CA2355978698
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661638A= , CM000682.2:g.23661638A= GRCh38
NC_000020.10:g.23642275A= , CM000682.1:g.23642275A= GRCh37
NC_000020.9:g.23590275A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.268A=