Canonical Allele Identifier: CA2284239322
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321213G= , CM000680.2:g.10321213G= GRCh38
NC_000018.9:g.10321210G= , CM000680.1:g.10321210G= GRCh37
NC_000018.8:g.10311210G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+935C=
XR_001753344.1:n.650+935C=
XR_001753345.1:n.908C=
XR_001753346.1:n.549+935C=