Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1672965190
- Species
- Homo sapiens
- Symbol
- rs1672965190
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HADHB
- Location
- 2:26284967
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000002.12:g.26284967T>C
- HGVS.c name
- ENSEMBL:ENST00000317799.10:c.1224+10T>C
- ENSEMBL:ENST00000405867.7:c.855+10T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:26243170...26290465 (47.30 kb)
- Assembly version
- Not Available
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