Canonical Allele Identifier: CA2200880783

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173323C= , CM000678.2:g.173323C=	GRCh38
NC_000016.9:g.223322C= , CM000678.1:g.223322C=	GRCh37
NC_000016.8:g.163322C=	NCBI36
NG_000006.1:g.34186C=
NG_059186.1:g.1673C=
NG_059271.1:g.5477C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.294C= MANE Select	ENSP00000251595.6:p.Asn98=
ENST00000251595.10:c.294C=	ENSP00000251595.6:p.Asn98=
ENST00000397806.1:c.198C=	ENSP00000380908.1:p.Asn66=
ENST00000482565.1:n.430C=
ENST00000484216.1:n.263C=
NM_000517.4:c.294C=	NP_000508.1:p.Asn98=
NM_000517.6:c.294C= MANE Select	NP_000508.1:p.Asn98=