Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2030004639
- Species
- Homo sapiens
- Symbol
- rs2030004639
- Category
- Variant
- Variant type
- SNP
- Overlaps
- AIFM1
- Location
- X:130130138
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)X:130130138T>C
- HGVS.c name
- ENSEMBL:ENST00000287295.8:c.1602A>G
- ENSEMBL:ENST00000319908.8:c.1596A>G
- HGVS.p name
- ENSP00000287295:p.Thr534=
- ENSP00000315122:p.Thr532=
- 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
- Viewer Help
Data currently unavailable; sequence viewer under construction