Canonical Allele Identifier: CA1899263542
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201859G= , CM000672.2:g.30201859G= GRCh38
NC_000010.10:g.30490788G= , CM000672.1:g.30490788G= GRCh37
NC_000010.9:g.30530794G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930791.1:n.1193-1628G=
XR_930791.2:n.1449-1628G=