Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs753889026
- Species
- Homo sapiens
- Symbol
- rs753889026
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MMP9
- Location
- 20:46010569
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)20:46010569C>A
- HGVS.c name
- ENSEMBL:ENST00000372330.3:c.458C>A
- RefSeq:NM_004994.3:c.458C>A
- HGVS.p name
- ENSP00000361405:p.Pro153Gln
- NP_004985:p.Pro153Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:46008908...46016561 (7.65 kb)
- Assembly version
- Not Available
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