Canonical Allele Identifier: CA2260478501
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42430300G= , CM000679.2:g.42430300G= GRCh38
NC_000017.10:g.40582318G= , CM000679.1:g.40582318G= GRCh37
NC_000017.9:g.37835844G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934762.1:n.505+5238G=
XR_934763.1:n.423+5238G=
XR_934765.1:n.255+5238G=
XR_001752890.2:n.326+5238G=
XR_002958124.1:n.382-5966G=
XR_934762.2:n.553+5238G=
XR_934765.2:n.257+5238G=