Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs207477955
- Species
- Homo sapiens
- Symbol
- rs207477955
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RTCB
- Location
- 22:32407123
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000022.11:g.32407123T>C
- HGVS.c name
- ENSEMBL:ENST00000216038.6:c.241-362A>G
- ENSEMBL:ENST00000476619.5:n.121+283A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr22:32387582...32412248 (24.67 kb)
- Assembly version
- Not Available
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