Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs901890792
- Species
- Homo sapiens
- Symbol
- rs901890792
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NKRF
- Location
- X:119605775
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000023.11:g.119605775G>C
- HGVS.c name
- ENSEMBL:ENST00000304449.8:c.-61C>G
- ENSEMBL:ENST00000542113.3:c.-114C>G
- HGVS.p name
- ENSP00000508667:p.Leu73=
- NP_001404819:p.Ser74Trp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:119588337...119606443 (18.11 kb)
- Assembly version
- Not Available
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