Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs200041385
- Species
- Homo sapiens
- Symbol
- rs200041385
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CCR9
- Location
- 3:45901277
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)3:45901277G>C
- HGVS.c name
- ENSEMBL:ENST00000355983.3:c.453G>C
- ENSEMBL:ENST00000357632.7:c.489G>C
- HGVS.p name
- ENSP00000348260:p.Leu151Phe
- ENSP00000350256:p.Leu163Phe
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:45884425...45903174 (18.75 kb)
- Assembly version
- Not Available
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