Canonical Allele Identifier: CA2200880661

Gene: HBA2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.173171G= , CM000678.2:g.173171G=	GRCh38
NC_000016.9:g.223170G= , CM000678.1:g.223170G=	GRCh37
NC_000016.8:g.163170G=	NCBI36
NG_000006.1:g.34034G=
NG_059186.1:g.1521G=
NG_059271.1:g.5325G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251595.11:c.142G= MANE Select	ENSP00000251595.6:p.Asp48=
ENST00000251595.10:c.142G=	ENSP00000251595.6:p.Asp48=
ENST00000397806.1:c.46G=	ENSP00000380908.1:p.Asp16=
ENST00000482565.1:n.278G=
ENST00000484216.1:n.111G=
NM_000517.4:c.142G=	NP_000508.1:p.Asp48=
NM_000517.6:c.142G= MANE Select	NP_000508.1:p.Asp48=