Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs145647753
- Species
- Homo sapiens
- Symbol
- rs145647753
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ANXA3
- Location
- 4:78591579
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000004.12:g.78591579G>A
- HGVS.c name
- ENSEMBL:ENST00000264908.11:c.439G>A
- ENSEMBL:ENST00000503570.6:c.322G>A
- HGVS.p name
- ENSP00000264908:p.Glu147Lys
- ENSP00000421015:p.Glu108Lys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:78551747...78610451 (58.70 kb)
- Assembly version
- Not Available
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