Canonical Allele Identifier: CA1949577634

Gene: HBG2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5254643A= , CM000673.2:g.5254643A=	GRCh38
NC_000011.9:g.5275873A= , CM000673.1:g.5275873A=	GRCh37
NC_000011.8:g.5232449A=	NCBI36
NG_000007.3:g.42973T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336906.6:c.86T= MANE Select	ENSP00000338082.4:p.Leu29=
ENST00000380252.6:c.-73-129T=	ENSP00000369602.2:n.-73-129T=
ENST00000380259.7:c.1632T=	ENSP00000369609.3:n.1632T=
ENST00000642908.1:c.86T=	ENSP00000495346.1:p.Leu29=
ENST00000647543.1:c.86T=	ENSP00000496470.1:p.Leu29=
ENST00000336906.4:c.86T=	ENSP00000338082.4:p.Leu29=
ENST00000380252.5:c.63-129T=	ENSP00000369602.1:n.63-129T=
ENST00000380259.6:c.86T=	ENSP00000369609.2:p.Leu29=
ENST00000444587.1:c.54+32T=	ENSP00000488218.1:n.54+32T=
ENST00000620888.4:c.86T=	ENSP00000479637.1:p.Leu29=
ENST00000624109.1:c.272A=	ENSP00000485458.1:p.Gln91=
NM_000184.2:c.86T=	NP_000175.1:p.Leu29=
NM_000184.3:c.86T= MANE Select	NP_000175.1:p.Leu29=