Canonical Allele Identifier: CA2200883035
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177012G= , CM000678.2:g.177012G= GRCh38
NC_000016.9:g.227011G= , CM000678.1:g.227011G= GRCh37
NC_000016.8:g.167011G= NCBI36
NG_000006.1:g.37875G=
NG_059186.1:g.5362G=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.179G= MANE Select ENSP00000322421.5:p.Gly60=
ENST00000397797.1:c.83G= ENSP00000380899.1:p.Gly28=
ENST00000472694.1:n.315G=
ENST00000487791.1:n.148G=
NM_000558.4:c.179G= NP_000549.1:p.Gly60=
NM_000558.5:c.179G= MANE Select NP_000549.1:p.Gly60=