Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs768205119
- Species
- Homo sapiens
- Symbol
- rs768205119
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TCERG1L
- Location
- 10:131260394
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000010.11:g.131260394C>T
- HGVS.c name
- ENSEMBL:ENST00000368642.4:c.721G>A
- RefSeq:XM_047424967.1:c.721G>A
- HGVS.p name
- ENSP00000357631:p.Ala241Thr
- XP_047280923:p.Ala241Thr
- 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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