Canonical Allele Identifier: CA2200880951

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173552C= , CM000678.2:g.173552C=	GRCh38
NC_000016.9:g.223551C= , CM000678.1:g.223551C=	GRCh37
NC_000016.8:g.163551C=	NCBI36
NG_000006.1:g.34415C=
NG_059186.1:g.1902C=
NG_059271.1:g.5706C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.381C= MANE Select	ENSP00000251595.6:p.Asp127=
ENST00000251595.10:c.381C=	ENSP00000251595.6:p.Asp127=
ENST00000397806.1:c.285C=	ENSP00000380908.1:p.Asp95=
ENST00000482565.1:n.517C=
NM_000517.4:c.381C=	NP_000508.1:p.Asp127=
NM_000517.6:c.381C= MANE Select	NP_000508.1:p.Asp127=