Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs750795944
- Species
- Homo sapiens
- Symbol
- rs750795944
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KTI12
- Location
- 1:52033339
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- NC_000001.11:g.52033339G>C
- HGVS.c name
- ENSEMBL:ENST00000371614.2:c.423C>G
- ENSEMBL:ENST00000371626.9:c.159-4709C>G
- HGVS.p name
- ENSP00000360676:p.Asp141Glu
- NP_612426:p.Asp141Glu
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction