Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1289941262
- Species
- Homo sapiens
- Symbol
- rs1289941262
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TSNAX
- Location
- 1:231564588
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- (GRCh38)1:231564588G>A
- HGVS.c name
- ENSEMBL:ENST00000366639.9:c.556G>A
- ENSEMBL:ENST00000475168.1:n.3693G>A
- HGVS.p name
- ENSP00000355599:p.Asp186Asn
- NP_005990:p.Asp186Asn
- 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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