Canonical Allele Identifier: CA1949567701
Gene: HBB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5226620_5226622delinsTCA , CM000673.2:g.5226620_5226622delinsTCA GRCh38
NC_000011.9:g.5247850_5247852delinsTCA , CM000673.1:g.5247850_5247852delinsTCA GRCh37
NC_000011.8:g.5204426_5204428delinsTCA NCBI36
NG_000007.3:g.70994_70996delinsTGA
NG_059281.1:g.5450_5452delinsTGA

Transcript Alleles

HGVS Amino-acid change
ENST00000647020.1:c.270_272delinsTGA ENSP00000494175.1:p.Ser90=
ENST00000335295.4:c.270_272delinsTGA MANE Select ENSP00000333994.3:p.Ser90=
ENST00000380315.2:c.270_272delinsTGA ENSP00000369671.2:p.Ser90=
ENST00000475226.1:n.202_204delinsTGA
ENST00000485743.1:n.321_323delinsTGA
ENST00000633227.1:c.*86_*88delinsTGA ENSP00000488004.1:n.*86_*88delinsTGA
NM_000518.4:c.270_272delinsTGA NP_000509.1:p.Ser90=
NM_000518.5:c.270_272delinsTGA MANE Select NP_000509.1:p.Ser90=