Canonical Allele Identifier: CA880474329
Gene:

Linked Data

dbSNP Id: rs1260710891

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20218143_20218161del , CM000681.2:g.20218143_20218161del GRCh38
NC_000019.9:g.20328952_20328970del , CM000681.1:g.20328952_20328970del GRCh37
NC_000019.8:g.20189952_20189970del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-841_619-823del
XR_936389.1:n.502-841_502-823del
XR_936390.1:n.511-841_511-823del
XR_936391.1:n.514-841_514-823del
XR_936392.1:n.514-841_514-823del
XR_936394.1:n.41-591_41-573del
XR_001754063.2:n.1506-841_1506-823del
XR_001754064.2:n.138-841_138-823del
XR_001754066.1:n.3912-841_3912-823del
XR_001754067.1:n.3912-841_3912-823del
XR_001754068.1:n.3912-841_3912-823del
XR_936394.2:n.41-591_41-573del
XR_936406.2:n.1411-841_1411-823del