Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs377461431
- Species
- Homo sapiens
- Symbol
- rs377461431
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PLAA
- Location
- 9:26913947
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant&splice region variant
- HGVS.g name
- (GRCh38)9:26913947C>T
- HGVS.c name
- ENSEMBL:ENST00000397292.8:c.1487G>A
- ENSEMBL:ENST00000487173.5:c.66G>A
- HGVS.p name
- ENSP00000380460:p.Gly496Asp
- ENSP00000429372:p.Gly496Asp
- 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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