Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs371366906
- Species
- Homo sapiens
- Symbol
- rs371366906
- Category
- Variant
- Variant type
- SNP
- Overlaps
- INHA
- Location
- 2:219572581
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)2:219572581C>T
- HGVS.c name
- ENSEMBL:ENST00000243786.3:c.207C>T
- ENSEMBL:ENST00000489456.1:n.286-2113C>T
- HGVS.p name
- ENSP00000243786:p.His69=
- NP_002182:p.His69=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:219569162...219575711 (6.55 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction