Canonical Allele Identifier: CA7770232
Gene: HBA1 HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.176800G>A , CM000678.2:g.176800G>A GRCh38
NC_000016.9:g.226799G>A , CM000678.1:g.226799G>A GRCh37
NC_000016.8:g.166799G>A NCBI36
NG_000006.1:g.37663G>A
NG_059186.1:g.5150G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320868.9:c.84G>A MANE Select ENSP00000322421.5:p.Glu28=
ENST00000397797.1:c.-2+38G>A ENSP00000380899.1:n.-2+38G>A
ENST00000472694.1:n.103G>A
ENST00000487791.1:n.53G>A
NM_000558.4:c.84G>A NP_000549.1:p.Glu28=
NM_000558.5:c.84G>A MANE Select NP_000549.1:p.Glu28=