Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1566719337
- Species
- Homo sapiens
- Symbol
- rs1566719337
- Category
- Variant
- Variant type
- SNP
- Overlaps
- VIPAS39
- Location
- 14:77428362
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- (GRCh38)14:77428362C>A
- HGVS.c name
- ENSEMBL:ENST00000448935.6:c.1314+8G>T
- ENSEMBL:ENST00000553888.5:c.1461+8G>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:77426675...77457952 (31.28 kb)
- Assembly version
- Not Available
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