Canonical Allele Identifier: CA1963376070
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759473A= , CM000673.2:g.34759473A= GRCh38
NC_000011.9:g.34781020A= , CM000673.1:g.34781020A= GRCh37
NC_000011.8:g.34737596A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+4866A=
XR_931188.1:n.693+4866A=
XR_931189.1:n.854+4866A=
XR_931190.1:n.639+4866A=
XR_931191.1:n.689+4866A=
XR_001748174.1:n.855+4866A=
XR_001748176.1:n.1016+4866A=
XR_002957246.1:n.639+4866A=