Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1373821788
- Species
- Homo sapiens
- Symbol
- rs1373821788
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HSD17B10
- Location
- X:53433812
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000023.11:g.53433812T>A
- HGVS.c name
- ENSEMBL:ENST00000168216.11:c.102A>T
- ENSEMBL:ENST00000375298.4:c.102A>T
- HGVS.p name
- ENSP00000168216:p.Gly34=
- ENSP00000364447:p.Gly34=
- 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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