Canonical Allele Identifier: CA2284239394
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321362A= , CM000680.2:g.10321362A= GRCh38
NC_000018.9:g.10321359A= , CM000680.1:g.10321359A= GRCh37
NC_000018.8:g.10311359A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935138.1:n.665+786T=
XR_001753344.1:n.650+786T=
XR_001753345.1:n.759T=
XR_001753346.1:n.549+786T=