Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs749449900
- Species
- Homo sapiens
- Symbol
- rs749449900
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E2F5
- Location
- 8:85177559
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- NC_000008.11:g.85177559G>A
- HGVS.c name
- ENSEMBL:ENST00000416274.7:c.139G>A
- ENSEMBL:ENST00000418930.6:c.139G>A
- HGVS.p name
- ENSP00000398124:p.Gly47Ser
- ENSP00000414312:p.Gly47Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:85177154...85217158 (40.00 kb)
- Assembly version
- Not Available
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