Canonical Allele Identifier: CA1949570989
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226997_5227000delinsTCTC , CM000673.2:g.5226997_5227000delinsTCTC GRCh38
NC_000011.9:g.5248227_5248230delinsTCTC , CM000673.1:g.5248227_5248230delinsTCTC GRCh37
NC_000011.8:g.5204803_5204806delinsTCTC NCBI36
NG_000007.3:g.70616_70619delinsGAGA
NG_059281.1:g.5072_5075delinsGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.22_25delinsGAGA ENSP00000494175.1:p.Glu8=
ENST00000335295.4:c.22_25delinsGAGA MANE Select ENSP00000333994.3:p.Glu8=
ENST00000380315.2:c.22_25delinsGAGA ENSP00000369671.2:p.Glu8=
ENST00000485743.1:n.73_76delinsGAGA
ENST00000633227.1:c.22_25delinsGAGA ENSP00000488004.1:p.Glu8=
NM_000518.4:c.22_25delinsGAGA NP_000509.1:p.Glu8=
NM_000518.5:c.22_25delinsGAGA MANE Select NP_000509.1:p.Glu8=