Canonical Allele Identifier: CA2200883267
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177328G= , CM000678.2:g.177328G= GRCh38
NC_000016.9:g.227327G= , CM000678.1:g.227327G= GRCh37
NC_000016.8:g.167327G= NCBI36
NG_000006.1:g.38191G=
NG_059186.1:g.5678G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.346G= MANE Select ENSP00000322421.5:p.Ala116=
ENST00000397797.1:c.250G= ENSP00000380899.1:p.Ala84=
ENST00000472694.1:n.482G=
NM_000558.4:c.346G= NP_000549.1:p.Ala116=
NM_000558.5:c.346G= MANE Select NP_000549.1:p.Ala116=