Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs761023207
- Species
- Homo sapiens
- Symbol
- rs761023207
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EMC3
- Location
- 3:9969742
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.9969742C>T
- HGVS.c name
- ENSEMBL:ENST00000245046.7:c.634G>A
- ENSEMBL:ENST00000470827.3:c.634G>A
- HGVS.p name
- ENSP00000245046:p.Ala212Thr
- ENSP00000474771:p.Ala212Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:9962682...10011202 (48.52 kb)
- Assembly version
- Not Available
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