Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs746966639
- Species
- Homo sapiens
- Symbol
- rs746966639
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ABHD8
- Location
- 19:17301585
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000019.10:g.17301585C>G
- HGVS.c name
- ENSEMBL:ENST00000247706.4:c.32G>C
- ENSEMBL:ENST00000593489.1:c.80G>C
- HGVS.p name
- ENSP00000247706:p.Cys11Ser
- ENSP00000468883:p.Cys27Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:17292131...17310236 (18.11 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction