chr11:5226936:A>T Detail (hg38) (HBB, LOC106099062, LOC107133510)

Information

Genome

Assembly Position
hg19 chr11:5,248,166-5,248,166 View the variant detail on this assembly version.
hg38 chr11:5,226,936-5,226,936

HGVS

Type Transcript Protein
RefSeq NM_000518.4:c.86T>A NP_000509.1:p.Leu29Gln
Ensemble ENST00000335295.4:c.86T>A ENST00000335295.4:p.Leu29Gln
ENST00000485743.1:c.86T>A ENST00000485743.1:p.Leu29Gln
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic; 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
Pathogenic 1986-01-01 no assertion criteria provided Heinz body anemia germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.360 Heinz Body Anemias NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000518.4(HBB):c.86T>A (p.Leu29Gln) AND HEMOGLOBIN ST. LOUIS ClinVar Detail
NM_000518.4(HBB):c.86T>A (p.Leu29Gln) AND Heinz body anemia 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
rs33916412 dbSNP
Genome
hg38
Position
chr11:5,226,936-5,226,936
Variant Type
snv
Reference Allele
A
Alternative Allele
T
Genome browser