Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs372223382
- Species
- Homo sapiens
- Symbol
- rs372223382
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FUCA1
- Location
- 1:23845781
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)1:23845781G>C
- HGVS.c name
- ENSEMBL:ENST00000374479.4:c.1335C>G
- RefSeq:NM_000147.5:c.1335C>G
- HGVS.p name
- ENSP00000363603:p.Pro445=
- NP_000138:p.Pro445=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:23845077...23868290 (23.21 kb)
- Assembly version
- Not Available
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