chr11:5248024:A>T Detail (hg19) (HBB, LOC106099062, LOC107133510)

Information

Genome

Assembly Position
hg19 chr11:5,248,024-5,248,024
hg38 chr11:5,226,794-5,226,794 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000518.4:c.98T>A NP_000509.1:p.Leu33Gln
Ensemble ENST00000647020.1:c.98T>A ENST00000647020.1:p.Leu33Gln
ENST00000485743.1:c.98T>A ENST00000485743.1:p.Leu33Gln
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Likely 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
other 2017-12-12 no assertion criteria provided germline Detail
Likely pathogenic 2020-05-19 criteria provided, single submitter not provided germline Detail
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
NM_000518.4(HBB):c.[295G>A;98T>A] AND HEMOGLOBIN MEDICINE LAKE ClinVar Detail
NM_000518.4(HBB):c.98T>A (p.Leu33Gln) AND not provided ClinVar 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
rs33948578 dbSNP
Genome
hg19
Position
chr11:5,248,024-5,248,024
Variant Type
snv
Reference Allele
A
Alternative Allele
T
Genome browser