Canonical Allele Identifier: CA2284239392
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321359T= , CM000680.2:g.10321359T= GRCh38
NC_000018.9:g.10321356T= , CM000680.1:g.10321356T= GRCh37
NC_000018.8:g.10311356T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935138.1:n.665+789A=
XR_001753344.1:n.650+789A=
XR_001753345.1:n.762A=
XR_001753346.1:n.549+789A=