Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs207466655
- Species
- Homo sapiens
- Symbol
- rs207466655
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GMDS
- Location
- 6:1641136
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000006.12:g.1641136G>C
- HGVS.c name
- ENSEMBL:ENST00000380805.6:n.1250-16596C>G
- ENSEMBL:ENST00000380815.5:c.988-16596C>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:1623806...2245605 (621.80 kb)
- Assembly version
- Not Available
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