Canonical Allele Identifier: CA2200880440

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.172994G= , CM000678.2:g.172994G=	GRCh38
NC_000016.9:g.222993G= , CM000678.1:g.222993G=	GRCh37
NC_000016.8:g.162993G=	NCBI36
NG_000006.1:g.33857G=
NG_059186.1:g.1344G=
NG_059271.1:g.5148G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.82G= MANE Select	ENSP00000251595.6:p.Glu28=
ENST00000251595.10:c.82G=	ENSP00000251595.6:p.Glu28=
ENST00000397806.1:c.-2+36G=	ENSP00000380908.1:n.-2+36G=
ENST00000482565.1:n.101G=
ENST00000484216.1:n.51G=
NM_000517.4:c.82G=	NP_000508.1:p.Glu28=
NM_000517.6:c.82G= MANE Select	NP_000508.1:p.Glu28=