Canonical Allele Identifier: CA1899263477
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201700C= , CM000672.2:g.30201700C= GRCh38
NC_000010.10:g.30490629C= , CM000672.1:g.30490629C= GRCh37
NC_000010.9:g.30530635C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930791.1:n.1193-1787C=
XR_930791.2:n.1449-1787C=