Linked Data
dbSNP Id:
rs1557042567
gnomAD v2:
X-48761963-C-G
gnomAD v4:
X-48904686-C-G
MyVariant Identifiers:
chrX:g.48761963C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48904686C>G , CM000685.2:g.48904686C>G | GRCh38 |
| NC_000023.10:g.48761963C>G , CM000685.1:g.48761963C>G | GRCh37 |
| NC_000023.9:g.48646907C>G | NCBI36 |
| NG_015967.1:g.11769C>G | |
| NG_034300.1:g.12273G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000247138.11:c.1163+60G>C MANE Select | ENSP00000247138.5:n.1163+60G>C | |
| ENST00000247138.10:c.1163+60G>C | ENSP00000247138.5:n.1163+60G>C | |
| ENST00000376515.8:c.561G>C | ENSP00000365698.3:p.Gly187= | |
| ENST00000376521.6:c.*41G>C | ENSP00000365704.1:n.*41G>C | |
| ENST00000376529.8:c.573+60G>C | ENSP00000365712.3:n.573+60G>C | |
| ENST00000413561.7:c.785G>C | ||
| ENST00000445167.7:c.633G>C | ENSP00000402726.2:p.Gly211= | |
| ENST00000452555.7:c.*41G>C | ENSP00000416002.2:n.*41G>C | |
| ENST00000616181.5:c.*41G>C | ENSP00000478617.1:n.*41G>C | |
| ENST00000635285.1:c.*41G>C | ENSP00000489484.1:n.*41G>C | |
| ENST00000635460.1:c.425-1221G>C | ||
| ENST00000635589.1:c.*41G>C | ENSP00000489197.1:n.*41G>C | |
| ENST00000635628.1:c.*1117G>C | ENSP00000489613.1:n.*1117G>C | |
| NM_001032289.2:c.633G>C | NP_001027460.1:p.Gly211= | |
| NM_001042498.2:c.*41G>C | NP_001035963.1:n.*41G>C | |
| NM_001282647.1:c.573+60G>C | NP_001269576.1:n.573+60G>C | |
| NM_001282648.1:c.561G>C | NP_001269577.1:p.Gly187= | |
| NM_001282649.1:c.*41G>C | NP_001269578.1:n.*41G>C | |
| NM_001282650.1:c.*41G>C | NP_001269579.1:n.*41G>C | |
| NM_001282651.1:c.*41G>C | NP_001269580.1:n.*41G>C | |
| NM_005660.2:c.1163+60G>C | NP_005651.1:n.1163+60G>C | |
| NM_005660.3:c.1163+60G>C MANE Select | NP_005651.1:n.1163+60G>C | |
| NM_001032289.3:c.633G>C | NP_001027460.1:p.Gly211= | |
| NM_001042498.3:c.*41G>C | NP_001035963.1:n.*41G>C | |
| NM_001282647.2:c.573+60G>C | NP_001269576.1:n.573+60G>C | |
| NM_001282649.2:c.*41G>C | NP_001269578.1:n.*41G>C | |
| NM_001282650.2:c.*41G>C | NP_001269579.1:n.*41G>C | |
| NM_001282651.2:c.*41G>C | NP_001269580.1:n.*41G>C | |
| NM_001282648.2:c.561G>C | NP_001269577.1:p.Gly187= |