Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs34670162
- Species
- Homo sapiens
- Symbol
- rs34670162
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CALCA
- Location
- 11:14968891
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)11:14968891C>A
- HGVS.c name
- ENSEMBL:ENST00000331587.9:c.334G>T
- ENSEMBL:ENST00000361010.7:c.228-1037G>T
- HGVS.p name
- ENSP00000331746:p.Gly112Trp
- ENSP00000379657:p.Gly112Trp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:14966622...14972354 (5.73 kb)
- Assembly version
- Not Available
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