Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1253623989
- Species
- Homo sapiens
- Symbol
- rs1253623989
- Category
- Variant
- Variant type
- SNP
- Overlaps
- UBE2H
- Location
- 7:129835010
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000007.14:g.129835010C>A
- HGVS.c name
- ENSEMBL:ENST00000355621.8:c.479G>T
- ENSEMBL:ENST00000473814.6:c.386G>T
- HGVS.p name
- ENSP00000347836:p.Gly160Val
- ENSP00000417681:p.Gly127Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:129830732...129952960 (122.23 kb)
- Assembly version
- Not Available
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