Canonical Allele Identifier: CA1949567951

Gene: HBB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226640G= , CM000673.2:g.5226640G=	GRCh38
NC_000011.9:g.5247870G= , CM000673.1:g.5247870G=	GRCh37
NC_000011.8:g.5204446G=	NCBI36
NG_000007.3:g.70976C=
NG_059281.1:g.5432C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647020.1:c.252C=	ENSP00000494175.1:p.Gly84=
ENST00000335295.4:c.252C= MANE Select	ENSP00000333994.3:p.Gly84=
ENST00000380315.2:c.252C=	ENSP00000369671.2:p.Gly84=
ENST00000475226.1:n.184C=
ENST00000485743.1:n.303C=
ENST00000633227.1:c.*68C=	ENSP00000488004.1:n.*68C=
NM_000518.4:c.252C=	NP_000509.1:p.Gly84=
NM_000518.5:c.252C= MANE Select	NP_000509.1:p.Gly84=