Linked Data
ClinVar Variation Id:
1103166
ClinVar RCV Id:
RCV001426751
dbSNP Id:
rs2147509679
gnomAD v4:
X-70027912-A-T
MyVariant Identifiers:
chrX:g.69247762A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.70027912A>T , CM000685.2:g.70027912A>T | GRCh38 |
| NC_000023.10:g.69247762A>T , CM000685.1:g.69247762A>T | GRCh37 |
| NC_000023.9:g.69164487A>T | NCBI36 |
| NG_009809.1:g.416852A>T | |
| NG_009809.2:g.416846A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374552.9:c.582A>T MANE Select | ENSP00000363680.4:p.Pro194= | |
| ENST00000374552.8:c.582A>T | ENSP00000363680.4:p.Pro194= | |
| ENST00000374553.6:c.582A>T | ENSP00000363681.2:p.Pro194= | |
| ENST00000503592.5:c.186A>T | ENSP00000423037.1:p.Pro62= | |
| ENST00000524573.5:c.582A>T | ENSP00000432585.1:p.Pro194= | |
| ENST00000616899.1:c.186A>T | ENSP00000481963.1:p.Pro62= | |
| NM_001005609.1:c.582A>T | NP_001005609.1:p.Pro194= | |
| NM_001005612.2:c.582A>T | NP_001005612.2:p.Pro194= | |
| NM_001399.4:c.582A>T | NP_001390.1:p.Pro194= | |
| XM_006724630.2:c.582A>T | XP_006724693.1:p.Pro194= | |
| XM_011530885.1:c.582A>T | XP_011529187.1:p.Pro194= | |
| XM_011530885.2:c.582A>T | XP_011529187.1:p.Pro194= | |
| XM_017029336.1:c.582A>T | XP_016884825.1:p.Pro194= | |
| NM_001399.5:c.582A>T MANE Select | NP_001390.1:p.Pro194= | |
| NM_001005609.2:c.582A>T | NP_001005609.1:p.Pro194= | |
| NM_001005612.3:c.582A>T | NP_001005612.2:p.Pro194= |