Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs757665228
- Species
- Homo sapiens
- Symbol
- rs757665228
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ZC3H10
- Location
- 12:56121640
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000012.12:g.56121640C>G
- HGVS.c name
- ENSEMBL:ENST00000257940.7:c.1078C>G
- ENSEMBL:ENST00000551790.5:c.-144+2489C>G
- HGVS.p name
- ENSP00000257940:p.Pro360Ala
- NP_001290054:p.Pro360Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:56118260...56127514 (9.25 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction