Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs367691817
- Species
- Homo sapiens
- Symbol
- rs367691817
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRATD1
- Location
- 2:14634723
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000002.12:g.14634723C>G
- HGVS.c name
- ENSEMBL:ENST00000295092.3:c.744C>G
- ENSEMBL:ENST00000331243.4:c.744C>G
- HGVS.p name
- ENSP00000295092:p.His248Gln
- ENSP00000330681:p.His248Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:14632700...14651916 (19.22 kb)
- Assembly version
- Not Available
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