Canonical Allele Identifier: CA2002397673
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072406C= , CM000673.2:g.116072406C= GRCh38
NC_000011.9:g.115943124C= , CM000673.1:g.115943124C= GRCh37
NC_000011.8:g.115448334C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948055.1:n.192+608G=
XR_948056.1:n.311-5201G=
XR_948057.1:n.97+703G=
XR_001748401.1:n.192+608G=
XR_948055.2:n.192+608G=
XR_948056.2:n.314-5201G=
XR_948057.2:n.97+703G=