Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs371092213
- Species
- Homo sapiens
- Symbol
- rs371092213
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MMAB
- Location
- 12:109561829
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000012.12:g.109561829G>A
- HGVS.c name
- ENSEMBL:ENST00000420167.6:n.512C>T
- ENSEMBL:ENST00000537496.5:n.395C>T
- HGVS.p name
- ENSP00000445920:p.Val124=
- ENSP00000474582:p.Val72=
- 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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