Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs894288962
- Species
- Homo sapiens
- Symbol
- rs894288962
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TCERG1L
- Location
- 10:131116838
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000010.11:g.131116838C>G
- HGVS.c name
- ENSEMBL:ENST00000368642.4:c.1356G>C
- ENSEMBL:ENST00000483040.1:n.3218G>C
- HGVS.p name
- ENSP00000357631:p.Glu452Asp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr10:131092391...131311721 (219.33 kb)
- Assembly version
- Not Available
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