Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2084305079
- Species
- Homo sapiens
- Symbol
- rs2084305079
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MMAB
- Location
- 12:109568865
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- splice acceptor variant
- HGVS.g name
- NC_000012.12:g.109568865T>C
- HGVS.c name
- ENSEMBL:ENST00000420167.6:n.337-2A>G
- ENSEMBL:ENST00000503497.7:n.221-2A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:109553715...109573580 (19.87 kb)
- Assembly version
- Not Available
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