Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs201607111
- Species
- Homo sapiens
- Symbol
- rs201607111
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E2F1
- Location
- 20:33676909
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)20:33676909C>T
- HGVS.c name
- ENSEMBL:ENST00000343380.6:c.1137G>A
- RefSeq:NM_005225.3:c.1137G>A
- HGVS.p name
- ENSP00000345571:p.Ala379=
- NP_005216:p.Ala379=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:33675477...33686385 (10.91 kb)
- Assembly version
- Not Available
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