Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs267606232
- Species
- Homo sapiens
- Symbol
- rs267606232
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RTCB
- Location
- 22:32399645
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000022.11:g.32399645G>A
- HGVS.c name
- ENSEMBL:ENST00000216038.6:c.612C>T
- ENSEMBL:ENST00000476619.5:n.493C>T
- HGVS.p name
- ENSP00000216038:p.Pro204=
- NP_055121:p.Pro204=
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction