Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs374088703
- Species
- Homo sapiens
- Symbol
- rs374088703
- Category
- Variant
- Variant type
- SNP
- Overlaps
- INHA
- Location
- 2:219574867
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000002.12:g.219574867T>G
- HGVS.c name
- ENSEMBL:ENST00000243786.3:c.442T>G
- ENSEMBL:ENST00000489456.1:n.459T>G
- HGVS.p name
- ENSP00000243786:p.Ser148Ala
- NP_002182:p.Ser148Ala
- 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
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