Canonical Allele Identifier: CA2327233040
Gene:

Linked Data

dbSNP Id: rs2090126049

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20217936_20217938del , CM000681.2:g.20217936_20217938del GRCh38
NC_000019.9:g.20328745_20328747del , CM000681.1:g.20328745_20328747del GRCh37
NC_000019.8:g.20189745_20189747del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-618_619-616del
XR_936389.1:n.502-618_502-616del
XR_936390.1:n.511-618_511-616del
XR_936391.1:n.514-618_514-616del
XR_936392.1:n.514-618_514-616del
XR_936394.1:n.41-798_41-796del
XR_001754063.2:n.1506-618_1506-616del
XR_001754064.2:n.138-618_138-616del
XR_001754066.1:n.3912-618_3912-616del
XR_001754067.1:n.3912-618_3912-616del
XR_001754068.1:n.3912-618_3912-616del
XR_936394.2:n.41-798_41-796del
XR_936406.2:n.1411-618_1411-616del