Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3888468
- Species
- Homo sapiens
- Symbol
- rs3888468
- Category
- Variant
- Variant type
- SNP
- Overlaps
- KMT2C
- Location
- 7:152247896
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- (GRCh38)7:152247896C>A
- HGVS.c name
- ENSEMBL:ENST00000262189.11:c.2532+6G>T
- ENSEMBL:ENST00000355193.1:c.2751+6G>T
- HGVS.p name
- ENSP00000506784:p.Gly552=
- ENSP00000507332:p.Gly847=
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction