Canonical Allele Identifier: CA2284239412
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321395T= , CM000680.2:g.10321395T= GRCh38
NC_000018.9:g.10321392T= , CM000680.1:g.10321392T= GRCh37
NC_000018.8:g.10311392T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+753A=
XR_001753344.1:n.650+753A=
XR_001753345.1:n.726A=
XR_001753346.1:n.549+753A=