Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs12539800
- Species
- Homo sapiens
- Symbol
- rs12539800
- Category
- Variant
- Variant type
- SNP
- Overlaps
- UBE2H
- Location
- 7:129839298
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)7:129839298T>C
- HGVS.c name
- ENSEMBL:ENST00000355621.8:c.336A>G
- ENSEMBL:ENST00000472396.5:c.299-23A>G
- HGVS.p name
- ENSP00000347836:p.Leu112=
- ENSP00000417681:p.Leu79=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:129830732...129952960 (122.23 kb)
- Assembly version
- Not Available
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