Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2065895527
- Species
- Homo sapiens
- Symbol
- rs2065895527
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ATP6V0C
- Location
- 16:2519310
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)16:2519310C>G
- HGVS.c name
- ENSEMBL:ENST00000330398.9:c.172C>G
- ENSEMBL:ENST00000564973.1:c.43C>G
- HGVS.p name
- ENSP00000329757:p.Pro58Ala
- ENSP00000454597:p.Pro40Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:2513726...2520218 (6.49 kb)
- Assembly version
- Not Available
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