Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs766501807
- Species
- Homo sapiens
- Symbol
- rs766501807
- Category
- Variant
- Variant type
- SNP
- Overlaps
- WARS2
- Location
- 1:119076467
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:119076467G>C
- HGVS.c name
- ENSEMBL:ENST00000235521.5:c.231C>G
- ENSEMBL:ENST00000369426.9:c.231C>G
- HGVS.p name
- ENSP00000235521:p.His77Gln
- ENSP00000358434:p.His77Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:119031216...119140672 (109.46 kb)
- Assembly version
- Not Available
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