Canonical Allele Identifier: CA1963375994
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759386C= , CM000673.2:g.34759386C= GRCh38
NC_000011.9:g.34780933C= , CM000673.1:g.34780933C= GRCh37
NC_000011.8:g.34737509C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+4779C=
XR_931188.1:n.693+4779C=
XR_931189.1:n.854+4779C=
XR_931190.1:n.639+4779C=
XR_931191.1:n.689+4779C=
XR_001748174.1:n.855+4779C=
XR_001748176.1:n.1016+4779C=
XR_002957246.1:n.639+4779C=