All variants in the HBB gene

Information The variants shown are described using the NM_000518.4 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

Haplotype     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
+?/. _1 c.-82C>T - r.(?) p.(?) - VUS g.5248333G>A g.5227103G>A -32 (C>T) - HBB_001352 - data from Globin Gene Server (HbVar-2536), Eng B; Waye JS (E-4075-2010);HbVar A-2391-201, PubMed: Eng B - rs34500389 Germline - - - 0 - HbVar - Belinda Giardine and Ross Hardison
+/. - c.-82C>T - r.(=) p.(=) - pathogenic g.5248333G>A g.5227103G>A -32 (C>T) - HBB_001352 β-thalassaemia, Haemolytic anaemia, Ineffective erythropoiesis IthaNet-19 - - SUMMARY record - - - 0 - IthaNet - Petros Kountouris
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