Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs371113016
- Species
- Homo sapiens
- Symbol
- rs371113016
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HOXD1
- Location
- 2:176189253
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- non coding transcript exon variant
- HGVS.g name
- NC_000002.12:g.176189253A>G
- HGVS.c name
- ENSEMBL:ENST00000331462.6:c.452A>G
- ENSEMBL:ENST00000843190.1:n.116T>C
- HGVS.p name
- ENSP00000328598:p.Gln151Arg
- 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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