Canonical Allele Identifier: CA2200882860
Gene: HBA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176787A= , CM000678.2:g.176787A= GRCh38
NC_000016.9:g.226786A= , CM000678.1:g.226786A= GRCh37
NC_000016.8:g.166786A= NCBI36
NG_000006.1:g.37650A=
NG_059186.1:g.5137A=

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.71A= MANE Select ENSP00000322421.5:p.Glu24=
ENST00000397797.1:c.-2+25A= ENSP00000380899.1:n.-2+25A=
ENST00000472694.1:n.90A=
ENST00000487791.1:n.40A=
NM_000558.4:c.71A= NP_000549.1:p.Glu24=
NM_000558.5:c.71A= MANE Select NP_000549.1:p.Glu24=