Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs753761872
- Species
- Homo sapiens
- Symbol
- rs753761872
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MMP2
- Location
- 16:55485324
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)16:55485324C>T
- HGVS.c name
- ENSEMBL:ENST00000219070.9:c.555C>T
- ENSEMBL:ENST00000437642.6:c.405C>T
- HGVS.p name
- ENSP00000219070:p.Asp185=
- ENSP00000394237:p.Asp135=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:55389700...55506691 (116.99 kb)
- Assembly version
- Not Available
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