Canonical Allele Identifier: CA1963413427
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812701T= , CM000673.2:g.34812701T= GRCh38
NC_000011.9:g.34834248T= , CM000673.1:g.34834248T= GRCh37
NC_000011.8:g.34790824T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+58094T=
XR_931188.1:n.693+58094T=
XR_931189.1:n.854+58094T=
XR_931190.1:n.639+58094T=
XR_931191.1:n.689+58094T=
XR_001748174.1:n.855+58094T=
XR_001748176.1:n.1016+58094T=
XR_002957246.1:n.639+58094T=