Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs767694711
- Species
- Homo sapiens
- Symbol
- rs767694711
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KIF6
- Location
- 6:39720799
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)6:39720799C>A
- HGVS.c name
- ENSEMBL:ENST00000287152.12:c.79G>T
- ENSEMBL:ENST00000482238.5:n.174G>T
- HGVS.p name
- ENSP00000287152:p.Asp27Tyr
- NP_001338432:p.Asp27Tyr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:39329990...39725408 (395.42 kb)
- Assembly version
- Not Available
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