Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs763783083
- Species
- Homo sapiens
- Symbol
- rs763783083
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MMAB
- Location
- 12:109561795
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:109561795G>T
- HGVS.c name
- ENSEMBL:ENST00000420167.6:n.546C>A
- ENSEMBL:ENST00000537496.5:n.429C>A
- HGVS.p name
- ENSP00000445920:p.Arg136=
- ENSP00000474582:p.Arg84=
- 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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