Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs753612198
- Species
- Homo sapiens
- Symbol
- rs753612198
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC3A2
- Location
- 11:62888400
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)11:62888400C>T
- HGVS.c name
- ENSEMBL:ENST00000338663.12:c.1297C>T
- ENSEMBL:ENST00000377889.6:c.1414C>T
- HGVS.p name
- ENSP00000340815:p.Arg433Cys
- ENSP00000367121:p.Arg472Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:62856004...62888880 (32.88 kb)
- Assembly version
- Not Available
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