Canonical Allele Identifier: CA2200882932

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.176871C= , CM000678.2:g.176871C=	GRCh38
NC_000016.9:g.226870C= , CM000678.1:g.226870C=	GRCh37
NC_000016.8:g.166870C=	NCBI36
NG_000006.1:g.37734C=
NG_059186.1:g.5221C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320868.9:c.96-58C= MANE Select	ENSP00000322421.5:n.96-58C=
ENST00000397797.1:c.-1-58C=	ENSP00000380899.1:n.-1-58C=
ENST00000472694.1:n.174C=
ENST00000487791.1:n.65-58C=
NM_000558.4:c.96-58C=	NP_000549.1:n.96-58C=
NM_000558.5:c.96-58C= MANE Select	NP_000549.1:n.96-58C=