Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs746055933
- Species
- Homo sapiens
- Symbol
- rs746055933
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ABHD8
- Location
- 19:17294491
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000019.10:g.17294491G>T
- HGVS.c name
- ENSEMBL:ENST00000247706.4:c.946C>A
- ENSEMBL:ENST00000595444.1:c.214+1637G>T
- HGVS.p name
- ENSP00000247706:p.Arg316Ser
- NP_078803:p.Arg316Ser
- 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
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