Canonical Allele Identifier: CA2200883342

Gene: HBA1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.177432G= , CM000678.2:g.177432G=	GRCh38
NC_000016.9:g.227431G= , CM000678.1:g.227431G=	GRCh37
NC_000016.8:g.167431G=	NCBI36
NG_000006.1:g.38295G=
NG_059186.1:g.5782G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320868.9:c.*21G= MANE Select	ENSP00000322421.5:n.*21G=
ENST00000397797.1:c.*21G=	ENSP00000380899.1:n.*21G=
ENST00000472694.1:n.586G=
NM_000558.4:c.*21G=	NP_000549.1:n.*21G=
NM_000558.5:c.*21G= MANE Select	NP_000549.1:n.*21G=