Canonical Allele Identifier: CA1949564743
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225663_5225672delinsCTGGTGGGGT , CM000673.2:g.5225663_5225672delinsCTGGTGGGGT GRCh38
NC_000011.9:g.5246893_5246902delinsCTGGTGGGGT , CM000673.1:g.5246893_5246902delinsCTGGTGGGGT GRCh37
NC_000011.8:g.5203469_5203478delinsCTGGTGGGGT NCBI36
NG_000007.3:g.71944_71953delinsACCCCACCAG
NG_059281.1:g.6400_6409delinsACCCCACCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.370_379delinsACCCCACCAG ENSP00000494175.1:p.Thr124=
ENST00000335295.4:c.370_379delinsACCCCACCAG MANE Select ENSP00000333994.3:p.Thr124=
ENST00000475226.1:n.302_311delinsACCCCACCAG
ENST00000633227.1:c.*186_*195delinsACCCCACCAG ENSP00000488004.1:n.*186_*195delinsACCCCA...
NM_000518.4:c.370_379delinsACCCCACCAG NP_000509.1:p.Thr124=
NM_000518.5:c.370_379delinsACCCCACCAG MANE Select NP_000509.1:p.Thr124=