Canonical Allele Identifier: CA2200883238
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177293A= , CM000678.2:g.177293A= GRCh38
NC_000016.9:g.227292A= , CM000678.1:g.227292A= GRCh37
NC_000016.8:g.167292A= NCBI36
NG_000006.1:g.38156A=
NG_059186.1:g.5643A=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.311A= MANE Select ENSP00000322421.5:p.His104=
ENST00000397797.1:c.215A= ENSP00000380899.1:p.His72=
ENST00000472694.1:n.447A=
NM_000558.4:c.311A= NP_000549.1:p.His104=
NM_000558.5:c.311A= MANE Select NP_000549.1:p.His104=