Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2144321951
- Species
- Homo sapiens
- Symbol
- rs2144321951
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BCL2
- Location
- 18:63318209
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000018.10:g.63318209A>T
- HGVS.c name
- ENSEMBL:ENST00000333681.5:c.458T>A
- ENSEMBL:ENST00000398117.1:c.458T>A
- HGVS.p name
- ENSP00000329623:p.Phe153Tyr
- ENSP00000381185:p.Phe153Tyr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr18:63123346...63320128 (196.78 kb)
- Assembly version
- Not Available
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