Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs764783588
- Species
- Homo sapiens
- Symbol
- rs764783588
- Category
- Variant
- Variant type
- SNP
- Overlaps
- OBSL1
- Location
- 2:219570807
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)2:219570807C>G
- HGVS.c name
- ENSEMBL:ENST00000289656.3:c.-228+587G>C
- ENSEMBL:ENST00000373873.8:c.426G>C
- HGVS.p name
- ENSP00000362980:p.Gly142=
- ENSP00000362983:p.Gly142=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:219547206...219571859 (24.65 kb)
- Assembly version
- Not Available
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