Canonical Allele Identifier: CA2200882868
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176798G= , CM000678.2:g.176798G= GRCh38
NC_000016.9:g.226797G= , CM000678.1:g.226797G= GRCh37
NC_000016.8:g.166797G= NCBI36
NG_000006.1:g.37661G=
NG_059186.1:g.5148G=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.82G= MANE Select ENSP00000322421.5:p.Glu28=
ENST00000397797.1:c.-2+36G= ENSP00000380899.1:n.-2+36G=
ENST00000472694.1:n.101G=
ENST00000487791.1:n.51G=
NM_000558.4:c.82G= NP_000549.1:p.Glu28=
NM_000558.5:c.82G= MANE Select NP_000549.1:p.Glu28=