Canonical Allele Identifier: CA2200880934

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173528C= , CM000678.2:g.173528C=	GRCh38
NC_000016.9:g.223527C= , CM000678.1:g.223527C=	GRCh37
NC_000016.8:g.163527C=	NCBI36
NG_000006.1:g.34391C=
NG_059186.1:g.1878C=
NG_059271.1:g.5682C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.357C= MANE Select	ENSP00000251595.6:p.Thr119=
ENST00000251595.10:c.357C=	ENSP00000251595.6:p.Thr119=
ENST00000397806.1:c.261C=	ENSP00000380908.1:p.Thr87=
ENST00000482565.1:n.493C=
NM_000517.4:c.357C=	NP_000508.1:p.Thr119=
NM_000517.6:c.357C= MANE Select	NP_000508.1:p.Thr119=