Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1181710439
- Species
- Homo sapiens
- Symbol
- rs1181710439
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TPRKB
- Location
- 2:73734555
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)2:73734555A>C
- HGVS.c name
- ENSEMBL:ENST00000272424.11:c.15T>G
- ENSEMBL:ENST00000462166.1:n.119T>G
- HGVS.p name
- ENSP00000272424:p.His5Gln
- NP_001317317:p.His5Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:73729104...73737400 (8.30 kb)
- Assembly version
- Not Available
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