Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs756114134
- Species
- Homo sapiens
- Symbol
- rs756114134
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRMT61B
- Location
- 2:28851278
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000002.12:g.28851278A>G
- HGVS.c name
- ENSEMBL:ENST00000306108.10:c.1106T>C
- ENSEMBL:ENST00000419999.5:c.6T>C
- HGVS.p name
- ENSP00000302801:p.Leu369Pro
- ENSP00000405467:p.Thr2=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:28849821...28870309 (20.49 kb)
- Assembly version
- Not Available
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