Canonical Allele Identifier: CA2200880655

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173166A= , CM000678.2:g.173166A=	GRCh38
NC_000016.9:g.223165A= , CM000678.1:g.223165A=	GRCh37
NC_000016.8:g.163165A=	NCBI36
NG_000006.1:g.34029A=
NG_059186.1:g.1516A=
NG_059271.1:g.5320A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.137A= MANE Select	ENSP00000251595.6:p.His46=
ENST00000251595.10:c.137A=	ENSP00000251595.6:p.His46=
ENST00000397806.1:c.41A=	ENSP00000380908.1:p.His14=
ENST00000482565.1:n.273A=
ENST00000484216.1:n.106A=
NM_000517.4:c.137A=	NP_000508.1:p.His46=
NM_000517.6:c.137A= MANE Select	NP_000508.1:p.His46=