Canonical Allele Identifier: CA1963376135
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759522G= , CM000673.2:g.34759522G= GRCh38
NC_000011.9:g.34781069G= , CM000673.1:g.34781069G= GRCh37
NC_000011.8:g.34737645G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+4915G=
XR_931188.1:n.693+4915G=
XR_931189.1:n.854+4915G=
XR_931190.1:n.639+4915G=
XR_931191.1:n.689+4915G=
XR_001748174.1:n.855+4915G=
XR_001748176.1:n.1016+4915G=
XR_002957246.1:n.639+4915G=