Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2092137661
- Species
- Homo sapiens
- Symbol
- rs2092137661
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SNX12
- Location
- X:71062898
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)X:71062898T>C
- HGVS.c name
- ENSEMBL:ENST00000276105.3:c.205A>G
- ENSEMBL:ENST00000374274.8:c.217A>G
- HGVS.p name
- ENSP00000276105:p.Ser69Gly
- ENSP00000363392:p.Ser73Gly
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:71056332...71073426 (17.09 kb)
- Assembly version
- Not Available
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