Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs141133000
- Species
- Homo sapiens
- Symbol
- rs141133000
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CFP
- Location
- X:47624353
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)X:47624353C>T
- HGVS.c name
- ENSEMBL:ENST00000247153.7:c.1332G>A
- ENSEMBL:ENST00000396992.8:c.1332G>A
- HGVS.p name
- ENSP00000247153:p.Gly444=
- ENSP00000380189:p.Gly444=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:47623172...47630305 (7.13 kb)
- Assembly version
- Not Available
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