Variant #0000926209 (NC_000016.9:g.226692C>G, NM_000517.4:c.*3093C>G (HBA2))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.226692C>G
DNA change (hg38) -
Published as HBA1(NM_000558.5):c.-24C>G
ISCN -
DB-ID HBA1_004006
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0523 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBA2 NM_000517.4 -/. - c.*3093C>G - r.(=) p.(=)
HBA1 NM_000558.3 -/. - c.-24C>G - r.(?) p.(=)
HBQ1 NM_005331.4 -/. - c.-3794C>G - r.(?) p.(=)


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