Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs547818652
- Species
- Homo sapiens
- Symbol
- rs547818652
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SGCG
- Location
- 13:23320639
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000013.11:g.23320639T>C
- HGVS.c name
- ENSEMBL:ENST00000218867.4:c.581T>C
- ENSEMBL:ENST00000682775.1:c.2186-8524A>G
- HGVS.p name
- ENSP00000218867:p.Leu194Ser
- NP_001365174:p.Leu194Ser
- 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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