Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs374386420
- Species
- Homo sapiens
- Symbol
- rs374386420
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ABHD8
- Location
- 19:17301430
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)19:17301430C>G
- HGVS.c name
- ENSEMBL:ENST00000247706.4:c.187G>C
- ENSEMBL:ENST00000593489.1:c.235G>C
- HGVS.p name
- ENSP00000247706:p.Ala63Pro
- ENSP00000468883:p.Ala79Pro
- 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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