Canonical Allele Identifier: CA2341104158
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837425_50837426delinsGT , CM000681.2:g.50837425_50837426delinsGT GRCh38
NC_000019.9:g.51340681_51340682delinsGT , CM000681.1:g.51340681_51340682delinsGT GRCh37
NC_000019.8:g.56032493_56032494delinsGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_131203.1:n.213+6132_213+6133delinsGT
NR_131205.1:n.230+6132_230+6133delinsGT
XR_936030.1:n.298+6132_298+6133delinsGT
XR_936031.1:n.298+6132_298+6133delinsGT
XR_936032.1:n.298+6132_298+6133delinsGT
XR_936033.1:n.294+6132_294+6133delinsGT
XR_936035.1:n.281+6132_281+6133delinsGT