Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs370063423
- Species
- Homo sapiens
- Symbol
- rs370063423
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NUBPL
- Location
- 14:31562104
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000014.9:g.31562104A>G
- HGVS.c name
- ENSEMBL:ENST00000281081.12:c.145A>G
- ENSEMBL:ENST00000547839.5:n.187A>G
- HGVS.p name
- ENSP00000281081:p.Arg49Gly
- ENSP00000446511:p.Arg24Gly
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:31489956...31861224 (371.27 kb)
- Assembly version
- Not Available
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