Canonical Allele Identifier: CA2200880726

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173256A= , CM000678.2:g.173256A=	GRCh38
NC_000016.9:g.223255A= , CM000678.1:g.223255A=	GRCh37
NC_000016.8:g.163255A=	NCBI36
NG_000006.1:g.34119A=
NG_059186.1:g.1606A=
NG_059271.1:g.5410A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.227A= MANE Select	ENSP00000251595.6:p.Asp76=
ENST00000251595.10:c.227A=	ENSP00000251595.6:p.Asp76=
ENST00000397806.1:c.131A=	ENSP00000380908.1:p.Asp44=
ENST00000482565.1:n.363A=
ENST00000484216.1:n.196A=
NM_000517.4:c.227A=	NP_000508.1:p.Asp76=
NM_000517.6:c.227A= MANE Select	NP_000508.1:p.Asp76=