Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs747039801
- Species
- Homo sapiens
- Symbol
- rs747039801
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ECPAS
- Location
- 9:111389720
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)9:111389720C>A
- HGVS.c name
- ENSEMBL:ENST00000259335.8:c.3817G>T
- ENSEMBL:ENST00000338205.9:c.3283G>T
- HGVS.p name
- ENSP00000259335:p.Ala1273Ser
- ENSP00000339889:p.Ala1095Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:111360685...111484745 (124.06 kb)
- Assembly version
- Not Available
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