Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs763166427
- Species
- Homo sapiens
- Symbol
- rs763166427
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MDM1
- Location
- 12:68315171
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:68315171T>C
- HGVS.c name
- ENSEMBL:ENST00000303145.11:c.1276A>G
- ENSEMBL:ENST00000411698.6:c.1171A>G
- HGVS.p name
- ENSP00000302537:p.Thr426Ala
- ENSP00000391006:p.Thr391Ala
- 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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