Variant #0001081450 (NC_000016.9:g.?, NM_000558.3:c.? (HBA1))

Chromosome 16
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.?
DNA change (hg38) g.?
Published as -alpha4.2
ISCN -
DB-ID CRYM_000000 See all 128 reported entries
Variant remarks -
Reference PubMed: Liu 2026
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 8/7496 chromosomes
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2026-08-03 14:41:16 +02:00 (CEST)
Date last edited N/A




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBA1 NM_000558.3 +/. - c.? - r.? p.?


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