Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs538616734
- Species
- Homo sapiens
- Symbol
- rs538616734
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRCC1
- Location
- 8:85131847
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- NC_000008.11:g.85131847T>G
- HGVS.c name
- ENSEMBL:ENST00000360375.8:c.1854T>G
- ENSEMBL:ENST00000414626.2:c.1794T>G
- HGVS.p name
- ENSP00000353538:p.His618Gln
- ENSP00000394695:p.His598Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:85107215...85146080 (38.87 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction