Canonical Allele Identifier: CA2200880469

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173001T= , CM000678.2:g.173001T=	GRCh38
NC_000016.9:g.223000T= , CM000678.1:g.223000T=	GRCh37
NC_000016.8:g.163000T=	NCBI36
NG_000006.1:g.33864T=
NG_059186.1:g.1351T=
NG_059271.1:g.5155T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.89T= MANE Select	ENSP00000251595.6:p.Leu30=
ENST00000251595.10:c.89T=	ENSP00000251595.6:p.Leu30=
ENST00000397806.1:c.-2+43T=	ENSP00000380908.1:n.-2+43T=
ENST00000482565.1:n.108T=
ENST00000484216.1:n.58T=
NM_000517.4:c.89T=	NP_000508.1:p.Leu30=
NM_000517.6:c.89T= MANE Select	NP_000508.1:p.Leu30=