Canonical Allele Identifier: CA1899676335
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.31077342T= , CM000672.2:g.31077342T= GRCh38
NC_000010.10:g.31366271T= , CM000672.1:g.31366271T= GRCh37
NC_000010.9:g.31406277T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747409.2:n.2299-28597T=
XR_001747410.2:n.2299-28597T=
XR_930796.1:n.389-28597T=
XR_930796.2:n.878-28597T=