Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1558817897
- Species
- Homo sapiens
- Symbol
- rs1558817897
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TIA1
- Location
- 2:70224606
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- NC_000002.12:g.70224606A>G
- HGVS.c name
- ENSEMBL:ENST00000282574.8:c.422T>C
- ENSEMBL:ENST00000361692.4:c.363T>C
- HGVS.p name
- ENSP00000282574:p.Met141Thr
- ENSP00000354838:p.His121=
- 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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