Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs141456610
- Species
- Homo sapiens
- Symbol
- rs141456610
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NKRF
- Location
- X:119589490
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)X:119589490A>G
- HGVS.c name
- ENSEMBL:ENST00000304449.8:c.1935T>C
- ENSEMBL:ENST00000371527.1:c.2588T>C
- HGVS.p name
- ENSP00000304803:p.Leu645=
- ENSP00000360582:p.Leu863Ser
- 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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