Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs80257651
- Species
- Homo sapiens
- Symbol
- rs80257651
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GATB
- Location
- 4:151688404
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000004.12:g.151688404C>T
- HGVS.c name
- ENSEMBL:ENST00000263985.11:c.1331+226G>A
- ENSEMBL:ENST00000503160.5:n.1206+226G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:151670504...151761007 (90.50 kb)
- Assembly version
- Not Available
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