Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs752474657
- Species
- Homo sapiens
- Symbol
- rs752474657
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EIF5B
- Location
- 2:99337578
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)2:99337578G>C
- HGVS.c name
- ENSEMBL:ENST00000289371.11:c.24G>C
- ENSEMBL:ENST00000409705.5:c.-33+739C>G
- HGVS.p name
- ENSP00000289371:p.Lys8Asn
- ENSP00000478914:p.Lys8Asn
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:99337389...99401326 (63.94 kb)
- Assembly version
- Not Available
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