Canonical Allele Identifier: CA2284239443
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321455A= , CM000680.2:g.10321455A= GRCh38
NC_000018.9:g.10321452A= , CM000680.1:g.10321452A= GRCh37
NC_000018.8:g.10311452A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+693T=
XR_001753344.1:n.650+693T=
XR_001753345.1:n.666T=
XR_001753346.1:n.549+693T=