Canonical Allele Identifier: CA1949569994

Gene: HBB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226893G= , CM000673.2:g.5226893G=	GRCh38
NC_000011.9:g.5248123G= , CM000673.1:g.5248123G=	GRCh37
NC_000011.8:g.5204699G=	NCBI36
NG_000007.3:g.70723C=
NG_059281.1:g.5179C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647020.1:c.92+37C=	ENSP00000494175.1:n.92+37C=
ENST00000335295.4:c.92+37C= MANE Select	ENSP00000333994.3:n.92+37C=
ENST00000380315.2:c.92+37C=	ENSP00000369671.2:n.92+37C=
ENST00000485743.1:n.143+37C=
ENST00000633227.1:c.76+53C=	ENSP00000488004.1:n.76+53C=
NM_000518.4:c.92+37C=	NP_000509.1:n.92+37C=
NM_000518.5:c.92+37C= MANE Select	NP_000509.1:n.92+37C=