Canonical Allele Identifier: CA2341104341

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50837822_50837823delinsCT , CM000681.2:g.50837822_50837823delinsCT	GRCh38
NC_000019.9:g.51341078_51341079delinsCT , CM000681.1:g.51341078_51341079delinsCT	GRCh37
NC_000019.8:g.56032890_56032891delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_131203.1:n.213+6529_213+6530delinsCT
NR_131205.1:n.230+6529_230+6530delinsCT
XR_936030.1:n.298+6529_298+6530delinsCT
XR_936031.1:n.298+6529_298+6530delinsCT
XR_936032.1:n.298+6529_298+6530delinsCT
XR_936033.1:n.294+6529_294+6530delinsCT
XR_936035.1:n.281+6529_281+6530delinsCT