Canonical Allele Identifier: CA2260478461
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42430182G= , CM000679.2:g.42430182G= GRCh38
NC_000017.10:g.40582200G= , CM000679.1:g.40582200G= GRCh37
NC_000017.9:g.37835726G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934762.1:n.505+5120G=
XR_934763.1:n.423+5120G=
XR_934765.1:n.255+5120G=
XR_001752890.2:n.326+5120G=
XR_002958124.1:n.382-6084G=
XR_934762.2:n.553+5120G=
XR_934765.2:n.257+5120G=