Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs781503261
- Species
- Homo sapiens
- Symbol
- rs781503261
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MYO5C
- Location
- 15:52244353
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- NC_000015.10:g.52244353T>C
- HGVS.c name
- ENSEMBL:ENST00000261839.12:c.2390+3A>G
- ENSEMBL:ENST00000558902.5:n.2667+3A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:52192322...52295804 (103.48 kb)
- Assembly version
- Not Available
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