Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1465787576
- Species
- Homo sapiens
- Symbol
- rs1465787576
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RXYLT1
- Location
- 12:63780117
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- stop gained
- HGVS.g name
- NC_000012.12:g.63780117A>T
- HGVS.c name
- ENSEMBL:ENST00000261234.11:c.157A>T
- ENSEMBL:ENST00000536219.5:n.276A>T
- HGVS.p name
- ENSP00000261234:p.Arg53Ter
- XP_047284035:p.Arg53Ter
- 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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