Version: 7.5.0
Date: Fri Dec 13 2024 Allele/Variant
rs201672171
- Species
- Homo sapiens
- Symbol
- rs201672171
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NUP210L
- Location
- 1:154001018
- Nucleotide Change
G>T
- Most Severe Consequence
- See all consequences
- HGVS.g name
- NC_000001.11:g.154001018G>T
- HGVS.c name
- ENSEMBL:ENST00000271854.3:c.4931-5838C>A
- ENSEMBL:ENST00000368553.5:c.1730-5838C>A
- HGVS.p name
- ENSP00000357547:p.His1742Asn
- NP_997191:p.His1742Asn
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Assembly version
- Not Available
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Variant Molecular Consequences