Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs756147466
- Species
- Homo sapiens
- Symbol
- rs756147466
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TSEN15
- Location
- 1:184051822
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:184051822G>C
- HGVS.c name
- ENSEMBL:ENST00000361641.6:c.67G>C
- ENSEMBL:ENST00000367518.4:n.105G>C
- HGVS.p name
- ENSP00000355299:p.Gly23Arg
- ENSP00000402002:p.Gly23Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:184051651...184123978 (72.33 kb)
- Assembly version
- Not Available
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