chr11:5226635:A>G Detail (hg38) (HBB, LOC106099062, LOC107133510)

Information

Genome

Assembly Position
hg19 chr11:5,247,865-5,247,865 View the variant detail on this assembly version.
hg38 chr11:5,226,635-5,226,635

HGVS

Type Transcript Protein
RefSeq NM_000518.4:c.257T>C NP_000509.1:p.Phe86Ser
Ensemble ENST00000335295.4:c.257T>C ENST00000335295.4:p.Phe86Ser
ENST00000485743.1:c.257T>C ENST00000485743.1:p.Phe86Ser
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
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
Pathogenic 1967-09-29 no assertion criteria provided hemoglobinopathy germline Detail
Pathogenic 2022-05-04 criteria provided, single submitter not provided germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.263 Hemoglobinopathies NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000518.5(HBB):c.257T>C (p.Phe86Ser) AND Hemoglobinopathy ClinVar Detail
NM_000518.5(HBB):c.257T>C (p.Phe86Ser) AND not provided ClinVar 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
rs35693898 dbSNP
Genome
hg38
Position
chr11:5,226,635-5,226,635
Variant Type
snv
Reference Allele
A
Alternative Allele
G
Genome browser