Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs551873770
- Species
- Homo sapiens
- Symbol
- rs551873770
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ACOXL
- Location
- 2:110798641
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)2:110798641C>T
- HGVS.c name
- ENSEMBL:ENST00000340561.8:c.377C>T
- ENSEMBL:ENST00000389811.8:c.377C>T
- HGVS.p name
- ENSP00000343717:p.Ala126Val
- ENSP00000374461:p.Ala126Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:110732539...111118548 (386.01 kb)
- Assembly version
- Not Available
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