Canonical Allele Identifier: CA1963413329
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812533T= , CM000673.2:g.34812533T= GRCh38
NC_000011.9:g.34834080T= , CM000673.1:g.34834080T= GRCh37
NC_000011.8:g.34790656T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+57926T=
XR_931188.1:n.693+57926T=
XR_931189.1:n.854+57926T=
XR_931190.1:n.639+57926T=
XR_931191.1:n.689+57926T=
XR_001748174.1:n.855+57926T=
XR_001748176.1:n.1016+57926T=
XR_002957246.1:n.639+57926T=