Canonical Allele Identifier: CA2002397757
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072558G= , CM000673.2:g.116072558G= GRCh38
NC_000011.9:g.115943276G= , CM000673.1:g.115943276G= GRCh37
NC_000011.8:g.115448486G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948055.1:n.192+456C=
XR_948056.1:n.311-5353C=
XR_948057.1:n.97+551C=
XR_001748401.1:n.192+456C=
XR_948055.2:n.192+456C=
XR_948056.2:n.314-5353C=
XR_948057.2:n.97+551C=