Linked Data
dbSNP Id:
rs1343959899
gnomAD v3:
X-154380557-G-C
gnomAD v4:
X-154380557-G-C
MyVariant Identifiers:
chrX:g.154380557G>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154380557G>C , CM000685.2:g.154380557G>C | GRCh38 |
| NC_000023.10:g.153608917G>C , CM000685.1:g.153608917G>C | GRCh37 |
| NC_000023.9:g.153262111G>C | NCBI36 |
| NG_008677.1:g.11122G>C , LRG_745:g.11122G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682114.1:c.399+190G>C | ENSP00000507245.1:n.399+190G>C | |
| ENST00000682478.1:n.589+190G>C | ||
| ENST00000683576.1:n.589+190G>C | ||
| ENST00000683627.1:c.399+190G>C | ENSP00000507533.1:n.399+190G>C | |
| ENST00000684082.1:c.356+190G>C | ENSP00000508266.1:n.356+190G>C | |
| ENST00000684633.1:n.371+190G>C | ||
| ENST00000684678.1:c.395+190G>C | ENSP00000507059.1:n.395+190G>C | |
| ENST00000369842.9:c.399+190G>C MANE Select | ENSP00000358857.4:n.399+190G>C | |
| ENST00000369835.3:c.294+190G>C | ENSP00000358850.3:n.294+190G>C | |
| ENST00000369842.8:c.399+190G>C | ENSP00000358857.4:n.399+190G>C | |
| ENST00000428228.5:c.*304+190G>C | ENSP00000401081.1:n.*304+190G>C | |
| ENST00000468294.5:n.359+190G>C | ||
| ENST00000485261.1:n.589+190G>C | ||
| ENST00000486738.5:n.757+190G>C | ||
| ENST00000492448.1:n.382+190G>C | ||
| NM_000117.2:c.399+190G>C , LRG_745t1:c.399+190G>C | NP_000108.1:n.399+190G>C | |
| XM_024452349.1:c.405+190G>C | XP_024308117.1:n.405+190G>C | |
| NM_000117.3:c.399+190G>C MANE Select | NP_000108.1:n.399+190G>C |