Canonical Allele Identifier: CA2200880898

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173484T= , CM000678.2:g.173484T=	GRCh38
NC_000016.9:g.223483T= , CM000678.1:g.223483T=	GRCh37
NC_000016.8:g.163483T=	NCBI36
NG_000006.1:g.34347T=
NG_059186.1:g.1834T=
NG_059271.1:g.5638T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.313T= MANE Select	ENSP00000251595.6:p.Cys105=
ENST00000251595.10:c.313T=	ENSP00000251595.6:p.Cys105=
ENST00000397806.1:c.217T=	ENSP00000380908.1:p.Cys73=
ENST00000482565.1:n.449T=
NM_000517.4:c.313T=	NP_000508.1:p.Cys105=
NM_000517.6:c.313T= MANE Select	NP_000508.1:p.Cys105=