Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs371025308
- Species
- Homo sapiens
- Symbol
- rs371025308
- Category
- Variant
- Variant type
- SNP
- Overlaps
- UBE2M
- Location
- 19:58558348
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)19:58558348T>C
- HGVS.c name
- ENSEMBL:ENST00000253023.8:c.34A>G
- ENSEMBL:ENST00000595957.5:c.-258A>G
- HGVS.p name
- ENSP00000253023:p.Lys12Glu
- NP_003960:p.Lys12Glu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:58555712...58558954 (3.24 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction