Canonical Allele Identifier: CA1800799697
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88579780T= , CM000670.2:g.88579780T= GRCh38
NC_000008.10:g.89592009T= , CM000670.1:g.89592009T= GRCh37
NC_000008.9:g.89661125T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928383.1:n.329+8611A=
XR_001745651.2:n.1081+8611A=
XR_001745653.2:n.416+36970T=
XR_928383.3:n.1081+8611A=