Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs57834270
- Species
- Homo sapiens
- Symbol
- rs57834270
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NUP188
- Location
- 9:128947888
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)9:128947888G>A
- HGVS.c name
- ENSEMBL:ENST00000372577.2:c.32+137G>A
- ENSEMBL:ENST00000491990.5:n.45+137G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:128947699...129007096 (59.40 kb)
- Assembly version
- Not Available
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