Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs370435803
- Species
- Homo sapiens
- Symbol
- rs370435803
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HOXD1
- Location
- 2:176189954
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000002.12:g.176189954C>T
- HGVS.c name
- ENSEMBL:ENST00000331462.6:c.799C>T
- HGVS.p name
- ENSP00000328598:p.His267Tyr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:176188668...176190907 (2.24 kb)
- Assembly version
- Not Available
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