Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs886041974
- Species
- Homo sapiens
- Symbol
- rs886041974
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HSD17B10
- Location
- X:53431556
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)X:53431556T>C
- HGVS.c name
- ENSEMBL:ENST00000168216.11:c.634A>G
- ENSEMBL:ENST00000375298.4:c.*15A>G
- HGVS.p name
- ENSP00000168216:p.Lys212Glu
- ENSP00000364453:p.Lys203Glu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:53431258...53434376 (3.12 kb)
- Assembly version
- Not Available
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