Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs760337387
- Species
- Homo sapiens
- Symbol
- rs760337387
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SLC7A5
- Location
- 16:87869272
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)16:87869272T>C
- HGVS.c name
- ENSEMBL:ENST00000261622.5:c.151A>G
- RefSeq:NM_003486.7:c.151A>G
- HGVS.p name
- ENSP00000261622:p.Thr51Ala
- NP_003477:p.Thr51Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:87830016...87869507 (39.49 kb)
- Assembly version
- Not Available
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