Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs201244599
- Species
- Homo sapiens
- Symbol
- rs201244599
- Category
- Variant
- Variant type
- SNP
- Overlaps
- WDCP
- Location
- 2:24037858
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)2:24037858T>C
- HGVS.c name
- ENSEMBL:ENST00000295148.9:c.1637A>G
- ENSEMBL:ENST00000406895.3:c.1637A>G
- HGVS.p name
- ENSP00000295148:p.Lys546Arg
- ENSP00000385816:p.Lys546Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:24029347...24049575 (20.23 kb)
- Assembly version
- Not Available
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