Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs312186
- Species
- Homo sapiens
- Symbol
- rs312186
- Category
- Variant
- Variant type
- SNP
- Overlaps
- AP2S1
- Location
- 19:46839460
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- splice region variant&intron variant
- HGVS.g name
- NC_000019.10:g.46839460C>T
- HGVS.c name
- ENSEMBL:ENST00000263270.11:c.267+5G>A
- ENSEMBL:ENST00000352203.8:c.309+5G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:46838136...46850846 (12.71 kb)
- Assembly version
- Not Available
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