Canonical Allele Identifier: CA1949568714
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226710_5226722delinsACCTTAGGGTTGC , CM000673.2:g.5226710_5226722delinsACCTTAGGGTTGC GRCh38
NC_000011.9:g.5247940_5247952delinsACCTTAGGGTTGC , CM000673.1:g.5247940_5247952delinsACCTTAGGGTTGC GRCh37
NC_000011.8:g.5204516_5204528delinsACCTTAGGGTTGC NCBI36
NG_000007.3:g.70894_70906delinsGCAACCCTAAGGT
NG_059281.1:g.5350_5362delinsGCAACCCTAAGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.170_182delinsGCAACCCTAAGGT ENSP00000494175.1:p.Gly57=
ENST00000335295.4:c.170_182delinsGCAACCCTAAGGT MANE Select ENSP00000333994.3:p.Gly57=
ENST00000380315.2:c.170_182delinsGCAACCCTAAGGT ENSP00000369671.2:p.Gly57=
ENST00000475226.1:n.102_114delinsGCAACCCTAAGGT
ENST00000485743.1:n.221_233delinsGCAACCCTAAGGT
ENST00000633227.1:c.154_166delinsGCAACCCTAAGGT ENSP00000488004.1:p.Ala52=
NM_000518.4:c.170_182delinsGCAACCCTAAGGT NP_000509.1:p.Gly57=
NM_000518.5:c.170_182delinsGCAACCCTAAGGT MANE Select NP_000509.1:p.Gly57=