Linked Data
dbSNP Id:
rs936927832
gnomAD v4:
X-135985324-A-G
MyVariant Identifiers:
chrX:g.135985324A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.135985324A>G , CM000685.2:g.135985324A>G | GRCh38 |
| NC_000023.10:g.135067483A>G , CM000685.1:g.135067483A>G | GRCh37 |
| NC_000023.9:g.134895149A>G | NCBI36 |
| NG_017160.1:g.4898A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370701.6:c.-210A>G | ENSP00000359735.1:n.-210A>G | |
| ENST00000636092.1:c.-56-279A>G | ENSP00000490406.1:n.-56-279A>G | |
| ENST00000636347.1:c.-35-300A>G | ENSP00000490648.1:n.-35-300A>G | |
| ENST00000637195.1:c.-35-300A>G | ENSP00000490330.1:n.-35-300A>G | |
| ENST00000637234.1:c.-56-279A>G | ENSP00000490527.1:n.-56-279A>G | |
| ENST00000637581.1:c.-56-279A>G | ENSP00000490731.1:n.-56-279A>G | |
| XM_006724726.3:c.-205A>G | XP_006724789.1:n.-205A>G | |
| XM_017029223.2:c.-56-279A>G | XP_016884712.1:n.-56-279A>G | |
| XM_017029224.1:c.-56-279A>G | XP_016884713.1:n.-56-279A>G | |
| NM_001400909.1:c.-35-300A>G | NP_001387838.1:n.-35-300A>G | |
| NM_001400910.1:c.-56-279A>G | NP_001387839.1:n.-56-279A>G | |
| NM_001400911.1:c.-56-279A>G | NP_001387840.1:n.-56-279A>G |