Canonical Allele Identifier: CA2327233017
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20217885T= , CM000681.2:g.20217885T= GRCh38
NC_000019.9:g.20328694T= , CM000681.1:g.20328694T= GRCh37
NC_000019.8:g.20189694T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-569A=
XR_936389.1:n.502-569A=
XR_936390.1:n.511-569A=
XR_936391.1:n.514-569A=
XR_936392.1:n.514-569A=
XR_936394.1:n.41-849T=
XR_001754063.2:n.1506-569A=
XR_001754064.2:n.138-569A=
XR_001754066.1:n.3912-569A=
XR_001754067.1:n.3912-569A=
XR_001754068.1:n.3912-569A=
XR_936394.2:n.41-849T=
XR_936406.2:n.1411-569A=