Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs777844887
- Species
- Homo sapiens
- Symbol
- rs777844887
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CLEC3B
- Location
- 3:45026394
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- NC_000003.12:g.45026394G>A
- HGVS.c name
- ENSEMBL:ENST00000296130.5:c.32G>A
- ENSEMBL:ENST00000481405.1:n.226-9130G>A
- HGVS.p name
- ENSP00000296130:p.Cys11Tyr
- XP_016862605:p.Cys11Tyr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:45001548...45036071 (34.52 kb)
- Assembly version
- Not Available
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