Linked Data
dbSNP Id:
rs1557182231
gnomAD v2:
X-153607951-T-C
gnomAD v4:
X-154379591-T-C
MyVariant Identifiers:
chrX:g.153607951T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154379591T>C , CM000685.2:g.154379591T>C | GRCh38 |
| NC_000023.10:g.153607951T>C , CM000685.1:g.153607951T>C | GRCh37 |
| NC_000023.9:g.153261145T>C | NCBI36 |
| NG_008677.1:g.10156T>C , LRG_745:g.10156T>C | |
| NG_011506.1:g.56A>G | |
| NG_011506.2:g.48A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000682114.1:c.82+25T>C | ENSP00000507245.1:n.82+25T>C | |
| ENST00000682478.1:n.58+25T>C | ||
| ENST00000683576.1:n.58+25T>C | ||
| ENST00000683627.1:c.82+25T>C | ENSP00000507533.1:n.82+25T>C | |
| ENST00000684082.1:c.82+25T>C | ENSP00000508266.1:n.82+25T>C | |
| ENST00000684633.1:n.54+29T>C | ||
| ENST00000684678.1:c.78+29T>C | ENSP00000507059.1:n.78+29T>C | |
| ENST00000369842.9:c.82+25T>C MANE Select | ENSP00000358857.4:n.82+25T>C | |
| ENST00000369835.3:c.82+25T>C | ENSP00000358850.3:n.82+25T>C | |
| ENST00000369842.8:c.82+25T>C | ENSP00000358857.4:n.82+25T>C | |
| ENST00000428228.5:c.53+54T>C | ENSP00000401081.1:n.53+54T>C | |
| ENST00000468294.5:n.42+25T>C | ||
| ENST00000485261.1:n.163+25T>C | ||
| ENST00000486738.5:n.226+25T>C | ||
| ENST00000494443.5:n.139+25T>C | ||
| NM_000117.2:c.82+25T>C , LRG_745t1:c.82+25T>C | NP_000108.1:n.82+25T>C | |
| XM_024452349.1:c.-127+25T>C | XP_024308117.1:n.-127+25T>C | |
| NM_000117.3:c.82+25T>C MANE Select | NP_000108.1:n.82+25T>C |