Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs762457418
- Species
- Homo sapiens
- Symbol
- rs762457418
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MMAB
- Location
- 12:109557129
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:109557129C>T
- HGVS.c name
- ENSEMBL:ENST00000537496.5:n.762G>A
- ENSEMBL:ENST00000540016.5:c.496G>A
- HGVS.p name
- ENSP00000445920:p.Asp218Asn
- ENSP00000474582:p.Asp166Asn
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:109553715...109573580 (19.87 kb)
- Assembly version
- Not Available
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