Canonical Allele Identifier: CA1949570231
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226930_5226931delinsCT , CM000673.2:g.5226930_5226931delinsCT GRCh38
NC_000011.9:g.5248160_5248161delinsCT , CM000673.1:g.5248160_5248161delinsCT GRCh37
NC_000011.8:g.5204736_5204737delinsCT NCBI36
NG_000007.3:g.70685_70686delinsAG
NG_059281.1:g.5141_5142delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.91_92delinsAG ENSP00000494175.1:p.Arg31=
ENST00000335295.4:c.91_92delinsAG MANE Select ENSP00000333994.3:p.Arg31=
ENST00000380315.2:c.91_92delinsAG ENSP00000369671.2:p.Arg31=
ENST00000485743.1:n.142_143delinsAG
ENST00000633227.1:c.76+15_76+16delinsAG ENSP00000488004.1:n.76+15_76+16delinsAG
NM_000518.4:c.91_92delinsAG NP_000509.1:p.Arg31=
NM_000518.5:c.91_92delinsAG MANE Select NP_000509.1:p.Arg31=