Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs201653184
- Species
- Homo sapiens
- Symbol
- rs201653184
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MMP2
- Location
- 16:55485437
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000016.10:g.55485437G>A
- HGVS.c name
- ENSEMBL:ENST00000219070.9:c.658+10G>A
- ENSEMBL:ENST00000437642.6:c.508+10G>A
- HGVS.p name
- Not Available
- 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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