Canonical Allele Identifier: CA2200880694

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173215G= , CM000678.2:g.173215G=	GRCh38
NC_000016.9:g.223214G= , CM000678.1:g.223214G=	GRCh37
NC_000016.8:g.163214G=	NCBI36
NG_000006.1:g.34078G=
NG_059186.1:g.1565G=
NG_059271.1:g.5369G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.186G= MANE Select	ENSP00000251595.6:p.Lys62=
ENST00000251595.10:c.186G=	ENSP00000251595.6:p.Lys62=
ENST00000397806.1:c.90G=	ENSP00000380908.1:p.Lys30=
ENST00000482565.1:n.322G=
ENST00000484216.1:n.155G=
NM_000517.4:c.186G=	NP_000508.1:p.Lys62=
NM_000517.6:c.186G= MANE Select	NP_000508.1:p.Lys62=