Canonical Allele Identifier: CA2200882907

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.176840G= , CM000678.2:g.176840G=	GRCh38
NC_000016.9:g.226839G= , CM000678.1:g.226839G=	GRCh37
NC_000016.8:g.166839G=	NCBI36
NG_000006.1:g.37703G=
NG_059186.1:g.5190G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320868.9:c.95+29G= MANE Select	ENSP00000322421.5:n.95+29G=
ENST00000397797.1:c.-2+78G=	ENSP00000380899.1:n.-2+78G=
ENST00000472694.1:n.143G=
ENST00000487791.1:n.64+29G=
NM_000558.4:c.95+29G=	NP_000549.1:n.95+29G=
NM_000558.5:c.95+29G= MANE Select	NP_000549.1:n.95+29G=