Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs935187661
- Species
- Homo sapiens
- Symbol
- rs935187661
- Category
- Variant
- Variant type
- SNP
- Overlaps
- AIFM1
- Location
- X:130137525
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000023.11:g.130137525T>C
- HGVS.c name
- ENSEMBL:ENST00000287295.8:c.968-340A>G
- ENSEMBL:ENST00000319908.8:c.965-340A>G
- HGVS.p name
- ENSP00000446113:p.Asp323Gly
- NP_665811:p.Ile367Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:130124666...130165879 (41.21 kb)
- Assembly version
- Not Available
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