Canonical Allele Identifier: CA2327233197
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20218263T= , CM000681.2:g.20218263T= GRCh38
NC_000019.9:g.20329072T= , CM000681.1:g.20329072T= GRCh37
NC_000019.8:g.20190072T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_936388.1:n.619-947A=
XR_936389.1:n.502-947A=
XR_936390.1:n.511-947A=
XR_936391.1:n.514-947A=
XR_936392.1:n.514-947A=
XR_936394.1:n.41-471T=
XR_001754063.2:n.1506-947A=
XR_001754064.2:n.138-947A=
XR_001754066.1:n.3912-947A=
XR_001754067.1:n.3912-947A=
XR_001754068.1:n.3912-947A=
XR_936394.2:n.41-471T=
XR_936406.2:n.1411-947A=