Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1036092694
- Species
- Homo sapiens
- Symbol
- rs1036092694
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GATB
- Location
- 4:151760957
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:151760957C>A
- HGVS.c name
- ENSEMBL:ENST00000263985.11:c.26G>T
- ENSEMBL:ENST00000508611.1:c.26G>T
- HGVS.p name
- ENSP00000263985:p.Gly9Val
- ENSP00000420831:p.Gly9Val
- 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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