Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1389889634
- Species
- Homo sapiens
- Symbol
- rs1389889634
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PHOX2B
- Location
- 4:41748543
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- non coding transcript exon variant
- HGVS.g name
- (GRCh38)4:41748543G>C
- HGVS.c name
- ENSEMBL:ENST00000226382.4:c.68C>G
- ENSEMBL:ENST00000508038.2:n.251G>C
- HGVS.p name
- ENSP00000226382:p.Thr23Ser
- NP_003915:p.Thr23Ser
- 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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