Canonical Allele Identifier: CA276416840
Gene: HBA1 HGNC NCBI

Linked Data

dbSNP Id: rs281864545
gnomAD v4: 16-177021-TG-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177023del , CM000678.2:g.177023del GRCh38
NC_000016.9:g.227022del , CM000678.1:g.227022del GRCh37
NC_000016.8:g.167022del NCBI36
NG_000006.1:g.37886del
NG_059186.1:g.5373del

Transcript Alleles

HGVS Amino-acid change
ENST00000320868.9:c.190del MANE Select ENSP00000322421.5:p.Ala64ProfsTer4
ENST00000397797.1:c.94del ENSP00000380899.1:p.Ala32ProfsTer4
ENST00000472694.1:n.326del
ENST00000487791.1:n.159del
NM_000558.4:c.190del NP_000549.1:p.Ala64ProfsTer4
NM_000558.5:c.190del MANE Select NP_000549.1:p.Ala64ProfsTer4