Canonical Allele Identifier: CA1899263545
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201866T= , CM000672.2:g.30201866T= GRCh38
NC_000010.10:g.30490795T= , CM000672.1:g.30490795T= GRCh37
NC_000010.9:g.30530801T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930791.1:n.1193-1621T=
XR_930791.2:n.1449-1621T=