Canonical Allele Identifier: CA2002397815
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072670C= , CM000673.2:g.116072670C= GRCh38
NC_000011.9:g.115943388C= , CM000673.1:g.115943388C= GRCh37
NC_000011.8:g.115448598C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948055.1:n.192+344G=
XR_948056.1:n.311-5465G=
XR_948057.1:n.97+439G=
XR_001748401.1:n.192+344G=
XR_948055.2:n.192+344G=
XR_948056.2:n.314-5465G=
XR_948057.2:n.97+439G=