Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2153113087
- Species
- Homo sapiens
- Symbol
- rs2153113087
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PHOX2B
- Location
- 4:41748606
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- NC_000004.12:g.41748606T>C
- HGVS.c name
- ENSEMBL:ENST00000226382.4:c.5A>G
- ENSEMBL:ENST00000508038.2:n.294+20T>C
- HGVS.p name
- ENSP00000226382:p.Tyr2Cys
- NP_003915:p.Tyr2Cys
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:41744082...41748725 (4.64 kb)
- Assembly version
- Not Available
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