Canonical Allele Identifier: CA1949569618

Gene: HBB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226793C= , CM000673.2:g.5226793C=	GRCh38
NC_000011.9:g.5248023C= , CM000673.1:g.5248023C=	GRCh37
NC_000011.8:g.5204599C=	NCBI36
NG_000007.3:g.70823G=
NG_059281.1:g.5279G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647020.1:c.99G=	ENSP00000494175.1:p.Leu33=
ENST00000335295.4:c.99G= MANE Select	ENSP00000333994.3:p.Leu33=
ENST00000380315.2:c.99G=	ENSP00000369671.2:p.Leu33=
ENST00000475226.1:n.31G=
ENST00000485743.1:n.150G=
ENST00000633227.1:c.83G=	ENSP00000488004.1:p.Trp28=
NM_000518.4:c.99G=	NP_000509.1:p.Leu33=
NM_000518.5:c.99G= MANE Select	NP_000509.1:p.Leu33=