Canonical Allele Identifier: CA1949583322

Gene: HBG1 HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5249146C= , CM000673.2:g.5249146C=	GRCh38
NC_000011.9:g.5270376C= , CM000673.1:g.5270376C=	GRCh37
NC_000011.8:g.5226952C=	NCBI36
NG_000007.3:g.48470G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330597.5:c.315+222G= (HBG1) MANE Select	ENSP00000327431.4:n.315+222G=
ENST00000642908.1:c.316-659G=	ENSP00000495346.1:n.316-659G=
ENST00000647543.1:c.379-659G=	ENSP00000496470.1:n.379-659G=
ENST00000648735.1:n.588G= (HBG1)
ENST00000330597.3:c.315+222G= (HBG1)	ENSP00000327431.3:n.315+222G=
ENST00000620888.4:c.316-659G= (HBG2)	ENSP00000479637.1:n.316-659G=
ENST00000623781.1:c.43-225C=	ENSP00000485381.1:n.43-225C=
ENST00000632727.1:c.*184+222G= (HBG1)	ENSP00000488759.1:n.*184+222G=
NM_000559.2:c.315+222G= (HBG1)	NP_000550.2:n.315+222G=
NM_000559.3:c.315+222G= (HBG1) MANE Select	NP_000550.2:n.315+222G=