Canonical Allele Identifier: CA1899263550
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201874A= , CM000672.2:g.30201874A= GRCh38
NC_000010.10:g.30490803A= , CM000672.1:g.30490803A= GRCh37
NC_000010.9:g.30530809A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930791.1:n.1193-1613A=
XR_930791.2:n.1449-1613A=