Canonical Allele Identifier: CA1963413384
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812629T= , CM000673.2:g.34812629T= GRCh38
NC_000011.9:g.34834176T= , CM000673.1:g.34834176T= GRCh37
NC_000011.8:g.34790752T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428897.2:n.579+58022T=
XR_931188.1:n.693+58022T=
XR_931189.1:n.854+58022T=
XR_931190.1:n.639+58022T=
XR_931191.1:n.689+58022T=
XR_001748174.1:n.855+58022T=
XR_001748176.1:n.1016+58022T=
XR_002957246.1:n.639+58022T=