Canonical Allele Identifier: CA1949568948
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226733_5226734delinsAT , CM000673.2:g.5226733_5226734delinsAT GRCh38
NC_000011.9:g.5247963_5247964delinsAT , CM000673.1:g.5247963_5247964delinsAT GRCh37
NC_000011.8:g.5204539_5204540delinsAT NCBI36
NG_000007.3:g.70882_70883delinsAT
NG_059281.1:g.5338_5339delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.158_159delinsAT ENSP00000494175.1:p.Asp53=
ENST00000335295.4:c.158_159delinsAT MANE Select ENSP00000333994.3:p.Asp53=
ENST00000380315.2:c.158_159delinsAT ENSP00000369671.2:p.Asp53=
ENST00000475226.1:n.90_91delinsAT
ENST00000485743.1:n.209_210delinsAT
ENST00000633227.1:c.142_143delinsAT ENSP00000488004.1:p.Met48=
NM_000518.4:c.158_159delinsAT NP_000509.1:p.Asp53=
NM_000518.5:c.158_159delinsAT MANE Select NP_000509.1:p.Asp53=