Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs150830660
- Species
- Homo sapiens
- Symbol
- rs150830660
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PLAA
- Location
- 9:26910436
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000009.12:g.26910436T>C
- HGVS.c name
- ENSEMBL:ENST00000397292.8:c.1559A>G
- ENSEMBL:ENST00000487173.5:c.138A>G
- HGVS.p name
- ENSP00000380460:p.Asn520Ser
- ENSP00000429372:p.Asn520Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:26903372...26947242 (43.87 kb)
- Assembly version
- Not Available
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