Canonical Allele Identifier: CA2200882935
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176878C= , CM000678.2:g.176878C= GRCh38
NC_000016.9:g.226877C= , CM000678.1:g.226877C= GRCh37
NC_000016.8:g.166877C= NCBI36
NG_000006.1:g.37741C=
NG_059186.1:g.5228C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.96-51C= MANE Select ENSP00000322421.5:n.96-51C=
ENST00000397797.1:c.-1-51C= ENSP00000380899.1:n.-1-51C=
ENST00000472694.1:n.181C=
ENST00000487791.1:n.65-51C=
NM_000558.4:c.96-51C= NP_000549.1:n.96-51C=
NM_000558.5:c.96-51C= MANE Select NP_000549.1:n.96-51C=