Linked Data
dbSNP Id:
rs1381314650
gnomAD v4:
X-154029761-G-A
MyVariant Identifiers:
chrX:g.154029761G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154029761G>A , CM000685.2:g.154029761G>A | GRCh38 |
| NC_000023.10:g.153295212G>A , CM000685.1:g.153295212G>A | GRCh37 |
| NC_000023.9:g.152948406G>A | NCBI36 |
| NG_007107.2:g.112367C>T | |
| NG_007107.3:g.112343C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303391.11:c.*606C>T MANE Plus Clinical | ENSP00000301948.6:n.*606C>T | |
| ENST00000453960.7:c.*606C>T MANE Select | ENSP00000395535.2:n.*606C>T | |
| ENST00000303391.10:c.*606C>T | ENSP00000301948.6:n.*606C>T | |
| ENST00000619732.4:c.*533C>T | ENSP00000480973.1:n.*533C>T | |
| NM_004992.3:c.*606C>T | NP_004983.1:n.*606C>T | |
| XM_005274681.3:c.*606C>T | XP_005274738.1:n.*606C>T | |
| XM_005274682.3:c.*606C>T | XP_005274739.1:n.*606C>T | |
| XM_005274683.3:c.*606C>T | XP_005274740.1:n.*606C>T | |
| XM_006724819.2:c.*606C>T | XP_006724882.1:n.*606C>T | |
| XM_011531166.1:c.*606C>T | XP_011529468.1:n.*606C>T | |
| XM_006724819.3:c.*606C>T | XP_006724882.1:n.*606C>T | |
| XM_011531166.2:c.*606C>T | XP_011529468.1:n.*606C>T | |
| XM_024452383.1:c.*606C>T | XP_024308151.1:n.*606C>T | |
| XM_024452384.1:c.*606C>T | XP_024308152.1:n.*606C>T | |
| NM_001110792.2:c.*606C>T MANE Select | NP_001104262.1:n.*606C>T | |
| NM_001316337.2:c.*606C>T | NP_001303266.1:n.*606C>T | |
| NM_001369391.2:c.*606C>T | NP_001356320.1:n.*606C>T | |
| NM_001369392.2:c.*606C>T | NP_001356321.1:n.*606C>T | |
| NM_001369393.2:c.*606C>T | NP_001356322.1:n.*606C>T | |
| NM_001369394.2:c.*606C>T | NP_001356323.1:n.*606C>T | |
| NM_001386137.1:c.*606C>T | NP_001373066.1:n.*606C>T | |
| NM_001386138.1:c.*606C>T | NP_001373067.1:n.*606C>T | |
| NM_001386139.1:c.*606C>T | NP_001373068.1:n.*606C>T | |
| NM_004992.4:c.*606C>T MANE Plus Clinical | NP_004983.1:n.*606C>T |