Canonical Allele Identifier: CA2200880460

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.172995A= , CM000678.2:g.172995A=	GRCh38
NC_000016.9:g.222994A= , CM000678.1:g.222994A=	GRCh37
NC_000016.8:g.162994A=	NCBI36
NG_000006.1:g.33858A=
NG_059186.1:g.1345A=
NG_059271.1:g.5149A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.83A= MANE Select	ENSP00000251595.6:p.Glu28=
ENST00000251595.10:c.83A=	ENSP00000251595.6:p.Glu28=
ENST00000397806.1:c.-2+37A=	ENSP00000380908.1:n.-2+37A=
ENST00000482565.1:n.102A=
ENST00000484216.1:n.52A=
NM_000517.4:c.83A=	NP_000508.1:p.Glu28=
NM_000517.6:c.83A= MANE Select	NP_000508.1:p.Glu28=