Canonical Allele Identifier: CA1949569635
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226795_5226829delinsGCAGCCTAAGGGTGGGAAAATAGACCAATAGGCAG , CM000673.2:g.5226795_5226829delinsGCAGCCTAAGGGTGGGAAAATAGACCAATAGGCAG GRCh38
NC_000011.9:g.5248025_5248059delinsGCAGCCTAAGGGTGGGAAAATAGACCAATAGGCAG , CM000673.1:g.5248025_5248059delinsGCAGCCTAAGGGTGGGAAAATAGACCAATAGGCAG GRCh37
NC_000011.8:g.5204601_5204635delinsGCAGCCTAAGGGTGGGAAAATAGACCAATAGGCAG NCBI36
NG_000007.3:g.70787_70821delinsCTGCCTATTGGTCTATTTTCCCACCCTTAGGCTGC
NG_059281.1:g.5243_5277delinsCTGCCTATTGGTCTATTTTCCCACCCTTAGGCTGC

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.93-30_97delinsCTGCCTATTGGTCTATTTTCCCACCCTTAGGCTGC
ENST00000335295.4:c.93-30_97delinsCTGCCTATTGGTCTATTTTCCCACCCTTAGGCTGC
ENST00000380315.2:c.93-30_97delinsCTGCCTATTGGTCTATTTTCCCACCCTTAGGCTGC
ENST00000485743.1:n.144-30_148delinsCTGCCTATTGGTCTATTTTCCCACCCTTAGGCTGC
ENST00000633227.1:c.77-30_81delinsCTGCCTATTGGTCTATTTTCCCACCCTTAGGCTGC
NM_000518.4:c.93-30_97delinsCTGCCTATTGGTCTATTTTCCCACCCTTAGGCTGC
NM_000518.5:c.93-30_97delinsCTGCCTATTGGTCTATTTTCCCACCCTTAGGCTGC