Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1297188253
- Species
- Homo sapiens
- Symbol
- rs1297188253
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC3A2
- Location
- 11:62882963
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)11:62882963C>G
- HGVS.c name
- ENSEMBL:ENST00000338663.12:c.654C>G
- ENSEMBL:ENST00000377889.6:c.771C>G
- HGVS.p name
- ENSP00000340815:p.Phe218Leu
- ENSP00000367121:p.Phe257Leu
- 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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