Canonical Allele Identifier: CA1949570426
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226947_5226954delinsACCAACTT , CM000673.2:g.5226947_5226954delinsACCAACTT GRCh38
NC_000011.9:g.5248177_5248184delinsACCAACTT , CM000673.1:g.5248177_5248184delinsACCAACTT GRCh37
NC_000011.8:g.5204753_5204760delinsACCAACTT NCBI36
NG_000007.3:g.70662_70669delinsAAGTTGGT
NG_059281.1:g.5118_5125delinsAAGTTGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.68_75delinsAAGTTGGT ENSP00000494175.1:p.Glu23=
ENST00000335295.4:c.68_75delinsAAGTTGGT MANE Select ENSP00000333994.3:p.Glu23=
ENST00000380315.2:c.68_75delinsAAGTTGGT ENSP00000369671.2:p.Glu23=
ENST00000485743.1:n.119_126delinsAAGTTGGT
ENST00000633227.1:c.68_75delinsAAGTTGGT ENSP00000488004.1:p.Glu23=
NM_000518.4:c.68_75delinsAAGTTGGT NP_000509.1:p.Glu23=
NM_000518.5:c.68_75delinsAAGTTGGT MANE Select NP_000509.1:p.Glu23=