chr11:5226762:C>T Detail (hg38) (HBB)

Information

Genome

Assembly Position
hg19 chr11:5,247,992-5,247,992 View the variant detail on this assembly version.
hg38 chr11:5,226,762-5,226,762

HGVS

Type Transcript Protein
RefSeq NM_000518.4:c.130G>A NP_000509.1:p.Glu44Lys
Ensemble ENST00000485743.1:c.130G>A ENST00000485743.1:p.Glu44Lys
ENST00000335295.4:c.130G>A ENST00000335295.4:p.Glu44Lys
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 141900 OMIM
HGNC 4827 HGNC
Ensembl ENSG00000244734 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC COSM3448555 COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.127 beta^0^ Thalassemia NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs33922842 dbSNP
Genome
hg38
Position
chr11:5,226,762-5,226,762
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Genome browser