Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs207460094
- Species
- Homo sapiens
- Symbol
- rs207460094
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SCMH1
- Location
- 1:41045911
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000001.11:g.41045911A>C
- HGVS.c name
- ENSEMBL:ENST00000326197.11:c.1468+496T>G
- ENSEMBL:ENST00000337495.9:c.1498+496T>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:41027202...41242306 (215.10 kb)
- Assembly version
- Not Available
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