Canonical Allele Identifier: CA2200880674

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173187C= , CM000678.2:g.173187C=	GRCh38
NC_000016.9:g.223186C= , CM000678.1:g.223186C=	GRCh37
NC_000016.8:g.163186C=	NCBI36
NG_000006.1:g.34050C=
NG_059186.1:g.1537C=
NG_059271.1:g.5341C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.158C= MANE Select	ENSP00000251595.6:p.Ser53=
ENST00000251595.10:c.158C=	ENSP00000251595.6:p.Ser53=
ENST00000397806.1:c.62C=	ENSP00000380908.1:p.Ser21=
ENST00000482565.1:n.294C=
ENST00000484216.1:n.127C=
NM_000517.4:c.158C=	NP_000508.1:p.Ser53=
NM_000517.6:c.158C= MANE Select	NP_000508.1:p.Ser53=