Canonical Allele Identifier: CA2002397744
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072533G= , CM000673.2:g.116072533G= GRCh38
NC_000011.9:g.115943251G= , CM000673.1:g.115943251G= GRCh37
NC_000011.8:g.115448461G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948055.1:n.192+481C=
XR_948056.1:n.311-5328C=
XR_948057.1:n.97+576C=
XR_001748401.1:n.192+481C=
XR_948055.2:n.192+481C=
XR_948056.2:n.314-5328C=
XR_948057.2:n.97+576C=