Canonical Allele Identifier: CA1949569013

Gene: HBB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226739A= , CM000673.2:g.5226739A=	GRCh38
NC_000011.9:g.5247969A= , CM000673.1:g.5247969A=	GRCh37
NC_000011.8:g.5204545A=	NCBI36
NG_000007.3:g.70877T=
NG_059281.1:g.5333T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647020.1:c.153T=	ENSP00000494175.1:p.Thr51=
ENST00000335295.4:c.153T= MANE Select	ENSP00000333994.3:p.Thr51=
ENST00000380315.2:c.153T=	ENSP00000369671.2:p.Thr51=
ENST00000475226.1:n.85T=
ENST00000485743.1:n.204T=
ENST00000633227.1:c.137T=	ENSP00000488004.1:p.Leu46=
NM_000518.4:c.153T=	NP_000509.1:p.Thr51=
NM_000518.5:c.153T= MANE Select	NP_000509.1:p.Thr51=