Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs756219488
- Species
- Homo sapiens
- Symbol
- rs756219488
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LIFR
- Location
- 5:38528808
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:38528808T>G
- HGVS.c name
- ENSEMBL:ENST00000263409.8:c.175A>C
- ENSEMBL:ENST00000453190.7:c.175A>C
- HGVS.p name
- ENSP00000263409:p.Asn59His
- ENSP00000398368:p.Asn59His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:38474668...38608403 (133.74 kb)
- Assembly version
- Not Available
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