Canonical Allele Identifier: CA2200880989

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173600A= , CM000678.2:g.173600A=	GRCh38
NC_000016.9:g.223599A= , CM000678.1:g.223599A=	GRCh37
NC_000016.8:g.163599A=	NCBI36
NG_000006.1:g.34463A=
NG_059186.1:g.1950A=
NG_059271.1:g.5754A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.429A= MANE Select	ENSP00000251595.6:p.Ter143=
ENST00000251595.10:c.429A=	ENSP00000251595.6:p.Ter143=
ENST00000397806.1:c.333A=	ENSP00000380908.1:p.Ter111=
ENST00000482565.1:n.565A=
NM_000517.4:c.429A=	NP_000508.1:p.Ter143=
NM_000517.6:c.429A= MANE Select	NP_000508.1:p.Ter143=