Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs73487878
- Species
- Homo sapiens
- Symbol
- rs73487878
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC3A2
- Location
- 11:62881276
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000011.10:g.62881276C>T
- HGVS.c name
- ENSEMBL:ENST00000338663.12:c.253C>T
- ENSEMBL:ENST00000377889.6:c.370C>T
- HGVS.p name
- ENSP00000340815:p.Leu85=
- ENSP00000367121:p.Leu124=
- 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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