Canonical Allele Identifier: CA2200883089

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.177088C= , CM000678.2:g.177088C=	GRCh38
NC_000016.9:g.227087C= , CM000678.1:g.227087C=	GRCh37
NC_000016.8:g.167087C=	NCBI36
NG_000006.1:g.37951C=
NG_059186.1:g.5438C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320868.9:c.255C= MANE Select	ENSP00000322421.5:p.Ser85=
ENST00000397797.1:c.159C=	ENSP00000380899.1:p.Ser53=
ENST00000472694.1:n.391C=
ENST00000487791.1:n.224C=
NM_000558.4:c.255C=	NP_000549.1:p.Ser85=
NM_000558.5:c.255C= MANE Select	NP_000549.1:p.Ser85=