Canonical Allele Identifier: CA1949570419

Gene: HBB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5226947A= , CM000673.2:g.5226947A=	GRCh38
NC_000011.9:g.5248177A= , CM000673.1:g.5248177A=	GRCh37
NC_000011.8:g.5204753A=	NCBI36
NG_000007.3:g.70669T=
NG_059281.1:g.5125T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647020.1:c.75T=	ENSP00000494175.1:p.Gly25=
ENST00000335295.4:c.75T= MANE Select	ENSP00000333994.3:p.Gly25=
ENST00000380315.2:c.75T=	ENSP00000369671.2:p.Gly25=
ENST00000485743.1:n.126T=
ENST00000633227.1:c.75T=	ENSP00000488004.1:p.Gly25=
NM_000518.4:c.75T=	NP_000509.1:p.Gly25=
NM_000518.5:c.75T= MANE Select	NP_000509.1:p.Gly25=