Canonical Allele Identifier: CA2327233089
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20218014A= , CM000681.2:g.20218014A= GRCh38
NC_000019.9:g.20328823A= , CM000681.1:g.20328823A= GRCh37
NC_000019.8:g.20189823A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-698T=
XR_936389.1:n.502-698T=
XR_936390.1:n.511-698T=
XR_936391.1:n.514-698T=
XR_936392.1:n.514-698T=
XR_936394.1:n.41-720A=
XR_001754063.2:n.1506-698T=
XR_001754064.2:n.138-698T=
XR_001754066.1:n.3912-698T=
XR_001754067.1:n.3912-698T=
XR_001754068.1:n.3912-698T=
XR_936394.2:n.41-720A=
XR_936406.2:n.1411-698T=