Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1897637160
- Species
- Homo sapiens
- Symbol
- rs1897637160
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RXYLT1
- Location
- 12:63780067
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:63780067C>T
- HGVS.c name
- ENSEMBL:ENST00000261234.11:c.107C>T
- ENSEMBL:ENST00000536219.5:n.226C>T
- HGVS.p name
- ENSP00000261234:p.Pro36Leu
- XP_047284035:p.Pro36Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:63779833...63809792 (29.96 kb)
- Assembly version
- Not Available
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