Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs754566272
- Species
- Homo sapiens
- Symbol
- rs754566272
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRAT
- Location
- 4:154749087
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000004.12:g.154749087C>G
- HGVS.c name
- ENSEMBL:ENST00000336356.4:c.644C>G
- ENSEMBL:ENST00000502474.5:n.439C>G
- HGVS.p name
- ENSP00000337224:p.Thr215Ser
- ENSP00000426761:p.Thr215Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:154626945...154753120 (126.18 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction