Variant #0000925435 (NC_000011.9:g.5271063C>T, NM_000184.2:c.*3444G>A (HBG2))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.5271063C>T
DNA change (hg38) -
Published as HBG1(NM_000559.2):c.-29G>A
ISCN -
DB-ID HBG1_003006
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) 0.15101 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     
HBG2 NM_000184.2 -?/. - c.*3444G>A - r.(=) p.(=)
HBG1 NM_000559.2 -?/. - c.-29G>A - r.(?) p.(=)


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