Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs751641627
- Species
- Homo sapiens
- Symbol
- rs751641627
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PPP2R1A
- Location
- 19:52215759
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000019.10:g.52215759C>G
- HGVS.c name
- ENSEMBL:ENST00000322088.11:c.808-20C>G
- ENSEMBL:ENST00000454220.7:c.928-20C>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:52170936...52229518 (58.58 kb)
- Assembly version
- Not Available
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