Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs202123982
- Species
- Homo sapiens
- Symbol
- rs202123982
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TIA1
- Location
- 2:70216486
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- (GRCh38)2:70216486C>G
- HGVS.c name
- ENSEMBL:ENST00000282574.8:c.597G>C
- ENSEMBL:ENST00000415783.6:c.564G>C
- HGVS.p name
- ENSP00000282574:p.Gln199His
- ENSP00000399567:p.Gln188His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:70209444...70248793 (39.35 kb)
- Assembly version
- Not Available
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