Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs562391447
- Species
- Homo sapiens
- Symbol
- rs562391447
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MCMDC2
- Location
- 8:66896897
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- (GRCh38)8:66896897A>G
- HGVS.c name
- ENSEMBL:ENST00000313616.5:c.1564A>G
- ENSEMBL:ENST00000396592.7:c.1564A>G
- HGVS.p name
- ENSP00000317234:p.Ile522Val
- ENSP00000379837:p.Ile522Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:66870749...66926382 (55.63 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction