Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs748533440
- Species
- Homo sapiens
- Symbol
- rs748533440
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TSNAX
- Location
- 1:231561210
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- non coding transcript exon variant
- HGVS.g name
- (GRCh38)1:231561210A>G
- HGVS.c name
- ENSEMBL:ENST00000366639.9:c.450A>G
- ENSEMBL:ENST00000413309.3:c.471A>G
- HGVS.p name
- ENSP00000355599:p.Lys150=
- ENSP00000397537:p.Lys157=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:231528541...231566524 (37.98 kb)
- Assembly version
- Not Available
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