Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs374491748
- Species
- Homo sapiens
- Symbol
- rs374491748
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KTI12
- Location
- 1:52033082
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)1:52033082C>T
- HGVS.c name
- ENSEMBL:ENST00000371614.2:c.680G>A
- ENSEMBL:ENST00000371626.9:c.159-4452G>A
- HGVS.p name
- ENSP00000360676:p.Arg227Gln
- NP_612426:p.Arg227Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:52032103...52033810 (1.71 kb)
- Assembly version
- Not Available
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