Canonical Allele Identifier: CA1949569218

Gene: HBB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226759A= , CM000673.2:g.5226759A=	GRCh38
NC_000011.9:g.5247989A= , CM000673.1:g.5247989A=	GRCh37
NC_000011.8:g.5204565A=	NCBI36
NG_000007.3:g.70857T=
NG_059281.1:g.5313T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647020.1:c.133T=	ENSP00000494175.1:p.Ser45=
ENST00000335295.4:c.133T= MANE Select	ENSP00000333994.3:p.Ser45=
ENST00000380315.2:c.133T=	ENSP00000369671.2:p.Ser45=
ENST00000475226.1:n.65T=
ENST00000485743.1:n.184T=
ENST00000633227.1:c.117T=	ENSP00000488004.1:p.Ser39=
NM_000518.4:c.133T=	NP_000509.1:p.Ser45=
NM_000518.5:c.133T= MANE Select	NP_000509.1:p.Ser45=