Canonical Allele Identifier: CA2246166013
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137866A= , CM000679.2:g.8137866A= GRCh38
NC_000017.10:g.8041184A= , CM000679.1:g.8041184A= GRCh37
NC_000017.9:g.7981909A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-983A=
XR_934203.1:n.70-1611A=
XR_934202.2:n.414-983A=