Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1556894569
- Species
- Homo sapiens
- Symbol
- rs1556894569
- Category
- Variant
- Variant type
- SNP
- Overlaps
- HSD17B10
- Location
- X:53431921
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000023.11:g.53431921G>T
- HGVS.c name
- ENSEMBL:ENST00000168216.11:c.487-15C>A
- ENSEMBL:ENST00000375298.4:c.486+67C>A
- HGVS.p name
- Not Available
- 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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