Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs16874289
- Species
- Homo sapiens
- Symbol
- rs16874289
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ENPP4
- Location
- 6:46143593
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000006.12:g.46143593T>G
- HGVS.c name
- ENSEMBL:ENST00000321037.5:c.1315T>G
- RefSeq:NM_014936.5:c.1315T>G
- HGVS.p name
- ENSP00000318066:p.Ser439Ala
- NP_055751:p.Ser439Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:46129989...46146688 (16.70 kb)
- Assembly version
- Not Available
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