Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs975063361
- Species
- Homo sapiens
- Symbol
- rs975063361
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CTU1
- Location
- 19:51098633
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)19:51098633G>A
- HGVS.c name
- ENSEMBL:ENST00000421832.3:c.1015C>T
- RefSeq:NM_145232.4:c.1015C>T
- HGVS.p name
- ENSP00000390011:p.Pro339Ser
- NP_660275:p.Pro339Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:51097606...51108409 (10.80 kb)
- Assembly version
- Not Available
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