Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1419447675
- Species
- Homo sapiens
- Symbol
- rs1419447675
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRSAM1
- Location
- 9:127473857
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)9:127473857G>A
- HGVS.c name
- ENSEMBL:ENST00000300417.11:c.676G>A
- ENSEMBL:ENST00000323301.8:c.676G>A
- HGVS.p name
- ENSP00000300417:p.Asp226Asn
- ENSP00000322937:p.Asp226Asn
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:127451486...127503501 (52.02 kb)
- Assembly version
- Not Available
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