Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs540938640
- Species
- Homo sapiens
- Symbol
- rs540938640
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SGCG
- Location
- 13:23320603
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)13:23320603T>G
- HGVS.c name
- ENSEMBL:ENST00000218867.4:c.579-34T>G
- ENSEMBL:ENST00000682775.1:c.2186-8488A>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr13:23160508...23325162 (164.65 kb)
- Assembly version
- Not Available
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