Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs34131679
- Species
- Homo sapiens
- Symbol
- rs34131679
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CD164
- Location
- 6:109375848
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000006.12:g.109375848C>A
- HGVS.c name
- ENSEMBL:ENST00000275080.11:c.331+2052G>T
- ENSEMBL:ENST00000310786.10:c.370+226G>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:109366514...109382467 (15.95 kb)
- Assembly version
- Not Available
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