Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1376969693
- Species
- Homo sapiens
- Symbol
- rs1376969693
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CALCA
- Location
- 11:14967810
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)11:14967810G>T
- HGVS.c name
- ENSEMBL:ENST00000361010.7:c.272C>A
- ENSEMBL:ENST00000469608.5:n.481C>A
- HGVS.p name
- ENSP00000354286:p.Thr91Asn
- ENSP00000417833:p.Thr91Asn
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:14966622...14972354 (5.73 kb)
- Assembly version
- Not Available
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