Canonical Allele Identifier: CA1949575356

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5253299G= , CM000673.2:g.5253299G=	GRCh38
NC_000011.9:g.5274529G= , CM000673.1:g.5274529G=	GRCh37
NC_000011.8:g.5231105G=	NCBI36
NG_000007.3:g.44317C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.422C= MANE Select	ENSP00000338082.4:p.Ala141=
ENST00000380252.6:c.257C=	ENSP00000369602.2:p.Ala86=
ENST00000642908.1:c.315+993C=	ENSP00000495346.1:n.315+993C=
ENST00000647543.1:c.378+44C=	ENSP00000496470.1:n.378+44C=
ENST00000336906.4:c.422C=	ENSP00000338082.4:p.Ala141=
ENST00000380252.5:c.392C=	ENSP00000369602.1:p.Ala131=
ENST00000380259.6:c.422C=	ENSP00000369609.2:p.Ala141=
ENST00000620888.4:c.315+993C=	ENSP00000479637.1:n.315+993C=
NM_000184.2:c.422C=	NP_000175.1:p.Ala141=
NM_000184.3:c.422C= MANE Select	NP_000175.1:p.Ala141=