Canonical Allele Identifier: CA2200883241
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177296G= , CM000678.2:g.177296G= GRCh38
NC_000016.9:g.227295G= , CM000678.1:g.227295G= GRCh37
NC_000016.8:g.167295G= NCBI36
NG_000006.1:g.38159G=
NG_059186.1:g.5646G=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.314G= MANE Select ENSP00000322421.5:p.Cys105=
ENST00000397797.1:c.218G= ENSP00000380899.1:p.Cys73=
ENST00000472694.1:n.450G=
NM_000558.4:c.314G= NP_000549.1:p.Cys105=
NM_000558.5:c.314G= MANE Select NP_000549.1:p.Cys105=