Canonical Allele Identifier: CA2200880933

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173527C= , CM000678.2:g.173527C=	GRCh38
NC_000016.9:g.223526C= , CM000678.1:g.223526C=	GRCh37
NC_000016.8:g.163526C=	NCBI36
NG_000006.1:g.34390C=
NG_059186.1:g.1877C=
NG_059271.1:g.5681C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.356C= MANE Select	ENSP00000251595.6:p.Thr119=
ENST00000251595.10:c.356C=	ENSP00000251595.6:p.Thr119=
ENST00000397806.1:c.260C=	ENSP00000380908.1:p.Thr87=
ENST00000482565.1:n.492C=
NM_000517.4:c.356C=	NP_000508.1:p.Thr119=
NM_000517.6:c.356C= MANE Select	NP_000508.1:p.Thr119=