Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs202229511
- Species
- Homo sapiens
- Symbol
- rs202229511
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RTCB
- Location
- 22:32395208
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000022.11:g.32395208C>T
- HGVS.c name
- ENSEMBL:ENST00000216038.6:c.997G>A
- RefSeq:NM_014306.5:c.997G>A
- HGVS.p name
- ENSP00000216038:p.Ala333Thr
- NP_055121:p.Ala333Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr22:32387582...32412248 (24.67 kb)
- Assembly version
- Not Available
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