Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs772296968
- Species
- Homo sapiens
- Symbol
- rs772296968
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MDM1
- Location
- 12:68325526
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:68325526T>C
- HGVS.c name
- ENSEMBL:ENST00000303145.11:c.548A>G
- ENSEMBL:ENST00000393543.7:c.*1908A>G
- HGVS.p name
- ENSP00000302537:p.Tyr183Cys
- ENSP00000446000:p.Tyr178Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:68272443...68332381 (59.94 kb)
- Assembly version
- Not Available
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