Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2129089876
- Species
- Homo sapiens
- Symbol
- rs2129089876
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KMT2C
- Location
- 7:152139731
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000007.14:g.152139731C>T
- HGVS.c name
- ENSEMBL:ENST00000262189.11:c.14404G>A
- ENSEMBL:ENST00000355193.1:c.14623G>A
- HGVS.p name
- ENSP00000262189:p.Gly4802Arg
- ENSP00000347325:p.Gly4875Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:152134922...152436644 (301.72 kb)
- Assembly version
- Not Available
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