Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs375522490
- Species
- Homo sapiens
- Symbol
- rs375522490
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BTG1
- Location
- 12:92144199
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:92144199T>C
- HGVS.c name
- ENSEMBL:ENST00000256015.5:c.397A>G
- ENSEMBL:ENST00000552315.1:n.423A>G
- HGVS.p name
- ENSP00000256015:p.Ser133Gly
- NP_001722:p.Ser133Gly
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:92140278...92145846 (5.57 kb)
- Assembly version
- Not Available
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