Canonical Allele Identifier: CA1963413387
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812633G= , CM000673.2:g.34812633G= GRCh38
NC_000011.9:g.34834180G= , CM000673.1:g.34834180G= GRCh37
NC_000011.8:g.34790756G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+58026G=
XR_931188.1:n.693+58026G=
XR_931189.1:n.854+58026G=
XR_931190.1:n.639+58026G=
XR_931191.1:n.689+58026G=
XR_001748174.1:n.855+58026G=
XR_001748176.1:n.1016+58026G=
XR_002957246.1:n.639+58026G=