Canonical Allele Identifier: CA1963413368
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812600G= , CM000673.2:g.34812600G= GRCh38
NC_000011.9:g.34834147G= , CM000673.1:g.34834147G= GRCh37
NC_000011.8:g.34790723G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+57993G=
XR_931188.1:n.693+57993G=
XR_931189.1:n.854+57993G=
XR_931190.1:n.639+57993G=
XR_931191.1:n.689+57993G=
XR_001748174.1:n.855+57993G=
XR_001748176.1:n.1016+57993G=
XR_002957246.1:n.639+57993G=