Canonical Allele Identifier: CA2695213070
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226989_5227001del , CM000673.2:g.5226989_5227001del GRCh38
NC_000011.9:g.5248219_5248231del , CM000673.1:g.5248219_5248231del GRCh37
NC_000011.8:g.5204795_5204807del NCBI36
NG_000007.3:g.70616_70628del
NG_059281.1:g.5072_5084del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647020.1:c.22_34del ENSP00000494175.1:p.Glu8LeufsTer8
ENST00000335295.4:c.22_34del MANE Select ENSP00000333994.3:p.Glu8LeufsTer8
ENST00000380315.2:c.22_34del ENSP00000369671.2:p.Glu8LeufsTer8
ENST00000485743.1:n.73_85del
ENST00000633227.1:c.22_34del ENSP00000488004.1:p.Glu8LeufsTer8
NM_000518.4:c.22_34del NP_000509.1:p.Glu8LeufsTer8
NM_000518.5:c.22_34del MANE Select NP_000509.1:p.Glu8LeufsTer8