Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs778660896
- Species
- Homo sapiens
- Symbol
- rs778660896
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GMFB
- Location
- 14:54483688
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000014.9:g.54483688T>C
- HGVS.c name
- ENSEMBL:ENST00000358056.8:c.83A>G
- ENSEMBL:ENST00000553333.1:c.119A>G
- HGVS.p name
- ENSP00000350757:p.Asn28Ser
- ENSP00000451920:p.Asn40Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:54474484...54489025 (14.54 kb)
- Assembly version
- Not Available
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