Canonical Allele Identifier: CA1963375891
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759292C= , CM000673.2:g.34759292C= GRCh38
NC_000011.9:g.34780839C= , CM000673.1:g.34780839C= GRCh37
NC_000011.8:g.34737415C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+4685C=
XR_931188.1:n.693+4685C=
XR_931189.1:n.854+4685C=
XR_931190.1:n.639+4685C=
XR_931191.1:n.689+4685C=
XR_001748174.1:n.855+4685C=
XR_001748176.1:n.1016+4685C=
XR_002957246.1:n.639+4685C=