chr11:5248233:C>G Detail (hg19) (HBB, LOC106099062, LOC107133510)

Information

Genome

Assembly Position
hg19 chr11:5,248,233-5,248,233
hg38 chr11:5,227,003-5,227,003 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000518.4:c.19G>C NP_000509.1:p.Glu7Gln
Ensemble ENST00000335295.4:c.19G>C ENST00000335295.4:p.Glu7Gln
ENST00000485743.1:c.19G>C ENST00000485743.1:p.Glu7Gln
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance other
Review star
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
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
other 2017-12-12 no assertion criteria provided germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.120 Malaria, resistance to NA CLINVAR Detail
0.578 Anemia, Sickle Cell NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000518.4(HBB):c.19G>C (p.Glu7Gln) AND HEMOGLOBIN MACHIDA ClinVar Detail
NA DisGeNET Detail
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
rs33930165 dbSNP
Genome
hg19
Position
chr11:5,248,233-5,248,233
Variant Type
snv
Reference Allele
C
Alternative Allele
G
Genome browser