Canonical Allele Identifier: CA2200880411

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.172985T= , CM000678.2:g.172985T=	GRCh38
NC_000016.9:g.222984T= , CM000678.1:g.222984T=	GRCh37
NC_000016.8:g.162984T=	NCBI36
NG_000006.1:g.33848T=
NG_059186.1:g.1335T=
NG_059271.1:g.5139T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.73T= MANE Select	ENSP00000251595.6:p.Tyr25=
ENST00000251595.10:c.73T=	ENSP00000251595.6:p.Tyr25=
ENST00000397806.1:c.-2+27T=	ENSP00000380908.1:n.-2+27T=
ENST00000482565.1:n.92T=
ENST00000484216.1:n.42T=
NM_000517.4:c.73T=	NP_000508.1:p.Tyr25=
NM_000517.6:c.73T= MANE Select	NP_000508.1:p.Tyr25=