Variant #0000281231 (NC_000011.9:g.5269584T>A, NM_000184.2:c.*4923A>T (HBG2))

Chromosome 11
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.5269584T>A
DNA change (hg38) g.5248354T>A
Published as HBG1(NM_000559.3):c.*5A>T
ISCN -
DB-ID HBG1_003002
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HBG2 NM_000184.2 -/. - c.*4923A>T - r.(=) p.(=)
HBG1 NM_000559.2 -/. - c.*5A>T - r.(=) p.(=)


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