Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs778730473
- Species
- Homo sapiens
- Symbol
- rs778730473
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CRNN
- Location
- 1:152410886
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- (GRCh38)1:152410886T>C
- HGVS.c name
- ENSEMBL:ENST00000271835.3:c.196A>G
- ENSEMBL:ENST00000411804.1:n.95-33958T>C
- HGVS.p name
- ENSP00000271835:p.Thr66Ala
- NP_057274:p.Thr66Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:152409243...152414263 (5.02 kb)
- Assembly version
- Not Available
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