Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs27399871
- Species
- Mus musculus
- Symbol
- rs27399871
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Phf21a
- Location
- 2:92076247
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCm39)2:92076247G>C
- HGVS.c name
- ENSEMBL:ENSMUST00000090586.1:c.153+15178G>C
- ENSEMBL:ENSMUST00000111291.1:c.153+15178G>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:92014451...92195011 (180.56 kb)
- Assembly version
- Not Available
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