Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1476916587
- Species
- Homo sapiens
- Symbol
- rs1476916587
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LHX8
- Location
- 1:75157080
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- (GRCh38)1:75157080G>C
- HGVS.c name
- ENSEMBL:ENST00000294638.9:c.994+4G>C
- RefSeq:NM_001001933.1:c.994+4G>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:75128434...75199454 (71.02 kb)
- Assembly version
- Not Available
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