Canonical Allele Identifier: CA2200880366

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.172976G= , CM000678.2:g.172976G=	GRCh38
NC_000016.9:g.222975G= , CM000678.1:g.222975G=	GRCh37
NC_000016.8:g.162975G=	NCBI36
NG_000006.1:g.33839G=
NG_059186.1:g.1326G=
NG_059271.1:g.5130G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.64G= MANE Select	ENSP00000251595.6:p.Ala22=
ENST00000251595.10:c.64G=	ENSP00000251595.6:p.Ala22=
ENST00000397806.1:c.-2+18G=	ENSP00000380908.1:n.-2+18G=
ENST00000482565.1:n.83G=
ENST00000484216.1:n.33G=
NM_000517.4:c.64G=	NP_000508.1:p.Ala22=
NM_000517.6:c.64G= MANE Select	NP_000508.1:p.Ala22=