Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1438760537
- Species
- Homo sapiens
- Symbol
- rs1438760537
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CCR9
- Location
- 3:45900828
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.45900828G>T
- HGVS.c name
- ENSEMBL:ENST00000355983.3:c.4G>T
- ENSEMBL:ENST00000357632.7:c.40G>T
- HGVS.p name
- ENSP00000348260:p.Ala2Ser
- ENSP00000350256:p.Ala14Ser
- 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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