Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs781405918
- Species
- Homo sapiens
- Symbol
- rs781405918
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KTI12
- Location
- 1:52033725
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- NC_000001.11:g.52033725C>A
- HGVS.c name
- ENSEMBL:ENST00000371614.2:c.37G>T
- ENSEMBL:ENST00000371626.9:c.159-5095G>T
- HGVS.p name
- ENSP00000360676:p.Gly13Cys
- NP_612426:p.Gly13Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:52032103...52033810 (1.71 kb)
- Assembly version
- Not Available
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