Canonical Allele Identifier: CA1899263465
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201669G= , CM000672.2:g.30201669G= GRCh38
NC_000010.10:g.30490598G= , CM000672.1:g.30490598G= GRCh37
NC_000010.9:g.30530604G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930791.1:n.1193-1818G=
XR_930791.2:n.1449-1818G=