Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1297109231
- Species
- Homo sapiens
- Symbol
- rs1297109231
- Category
- Variant
- Variant type
- SNP
- Overlaps
- AP2S1
- Location
- 19:46846117
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000019.10:g.46846117C>T
- HGVS.c name
- ENSEMBL:ENST00000263270.11:c.29G>A
- ENSEMBL:ENST00000352203.8:c.29G>A
- HGVS.p name
- ENSP00000263270:p.Arg10Gln
- ENSP00000263271:p.Arg10Gln
- 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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