Canonical Allele Identifier: CA2200883038

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.177016G= , CM000678.2:g.177016G=	GRCh38
NC_000016.9:g.227015G= , CM000678.1:g.227015G=	GRCh37
NC_000016.8:g.167015G=	NCBI36
NG_000006.1:g.37879G=
NG_059186.1:g.5366G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320868.9:c.183G= MANE Select	ENSP00000322421.5:p.Lys61=
ENST00000397797.1:c.87G=	ENSP00000380899.1:p.Lys29=
ENST00000472694.1:n.319G=
ENST00000487791.1:n.152G=
NM_000558.4:c.183G=	NP_000549.1:p.Lys61=
NM_000558.5:c.183G= MANE Select	NP_000549.1:p.Lys61=