Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2051551028
- Species
- Homo sapiens
- Symbol
- rs2051551028
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DNAAF19
- Location
- 17:44901670
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)17:44901670C>T
- HGVS.c name
- ENSEMBL:ENST00000357776.6:c.276+18C>T
- ENSEMBL:ENST00000410006.6:c.276+18C>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:44899142...44905390 (6.25 kb)
- Assembly version
- Not Available
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