Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs776118364
- Species
- Homo sapiens
- Symbol
- rs776118364
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E2F8
- Location
- 11:19225759
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- (GRCh38)11:19225759G>C
- HGVS.c name
- ENSEMBL:ENST00000250024.9:c.1999C>G
- ENSEMBL:ENST00000527884.5:c.1999C>G
- HGVS.p name
- ENSP00000250024:p.His667Asp
- ENSP00000434199:p.His667Asp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:19224063...19241655 (17.59 kb)
- Assembly version
- Not Available
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