Canonical Allele Identifier: CA2200883015
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176985A= , CM000678.2:g.176985A= GRCh38
NC_000016.9:g.226984A= , CM000678.1:g.226984A= GRCh37
NC_000016.8:g.166984A= NCBI36
NG_000006.1:g.37848A=
NG_059186.1:g.5335A=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.152A= MANE Select ENSP00000322421.5:p.His51=
ENST00000397797.1:c.56A= ENSP00000380899.1:p.His19=
ENST00000472694.1:n.288A=
ENST00000487791.1:n.121A=
NM_000558.4:c.152A= NP_000549.1:p.His51=
NM_000558.5:c.152A= MANE Select NP_000549.1:p.His51=