Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1393034082
- Species
- Homo sapiens
- Symbol
- rs1393034082
- Category
- Variant
- Variant type
- SNP
- Overlaps
- OGT
- Location
- X:71567519
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)X:71567519A>G
- HGVS.c name
- ENSEMBL:ENST00000373701.7:c.2579A>G
- ENSEMBL:ENST00000373719.8:c.2609A>G
- HGVS.p name
- ENSP00000362805:p.Asn860Ser
- ENSP00000362824:p.Asn870Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:71533087...71575892 (42.81 kb)
- Assembly version
- Not Available
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