Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs377744341
- Species
- Homo sapiens
- Symbol
- rs377744341
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PXK
- Location
- 3:58397638
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000003.12:g.58397638C>T
- HGVS.c name
- ENSEMBL:ENST00000302779.9:c.1018C>T
- ENSEMBL:ENST00000356151.7:c.1018C>T
- HGVS.p name
- ENSP00000305045:p.His340Tyr
- ENSP00000348472:p.His340Tyr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr3:58332880...58426127 (93.25 kb)
- Assembly version
- Not Available
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