Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs11556167
- Species
- Homo sapiens
- Symbol
- rs11556167
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GATB
- Location
- 4:151760894
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:151760894G>T
- HGVS.c name
- ENSEMBL:ENST00000263985.11:c.89C>A
- ENSEMBL:ENST00000503160.5:n.37C>A
- HGVS.p name
- ENSP00000263985:p.Ala30Asp
- ENSP00000420831:p.Ala30Asp
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction