Canonical Allele Identifier: CA2200882866
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176796C= , CM000678.2:g.176796C= GRCh38
NC_000016.9:g.226795C= , CM000678.1:g.226795C= GRCh37
NC_000016.8:g.166795C= NCBI36
NG_000006.1:g.37659C=
NG_059186.1:g.5146C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.80C= MANE Select ENSP00000322421.5:p.Ala27=
ENST00000397797.1:c.-2+34C= ENSP00000380899.1:n.-2+34C=
ENST00000472694.1:n.99C=
ENST00000487791.1:n.49C=
NM_000558.4:c.80C= NP_000549.1:p.Ala27=
NM_000558.5:c.80C= MANE Select NP_000549.1:p.Ala27=