Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2076707794
- Species
- Homo sapiens
- Symbol
- rs2076707794
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CTRB1
- Location
- 16:75223215
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)16:75223215C>A
- HGVS.c name
- ENSEMBL:ENST00000361017.9:c.311C>A
- ENSEMBL:ENST00000495583.1:c.383C>A
- HGVS.p name
- ENSP00000354294:p.Ala104Asp
- ENSP00000463301:p.Ala128Asp
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:75218988...75226338 (7.35 kb)
- Assembly version
- Not Available
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