Linked Data
ClinVar Variation Id:
2948905
ClinVar RCV Id:
RCV003801631
MyVariant Identifiers:
chrX:g.138644140T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.139561981T>C , CM000685.2:g.139561981T>C | GRCh38 |
| NC_000023.10:g.138644140T>C , CM000685.1:g.138644140T>C | GRCh37 |
| NC_000023.9:g.138471806T>C | NCBI36 |
| NG_007994.1:g.36246T>C , LRG_556:g.36246T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218099.7:c.1296T>C MANE Select | ENSP00000218099.2:p.Gly432= | |
| ENST00000643157.1:n.1723+240T>C | ||
| ENST00000218099.6:c.1296T>C | ENSP00000218099.2:p.Gly432= | |
| ENST00000394090.2:c.1182T>C | ENSP00000377650.2:p.Gly394= | |
| NM_000133.3:c.1296T>C , LRG_556t1:c.1296T>C | NP_000124.1:p.Gly432= | |
| NM_001313913.1:c.1182T>C | NP_001300842.1:p.Gly394= | |
| XM_005262397.3:c.1167T>C | XP_005262454.1:p.Gly389= | |
| XM_005262397.4:c.1167T>C | XP_005262454.1:p.Gly389= | |
| NM_000133.4:c.1296T>C MANE Select | NP_000124.1:p.Gly432= | |
| NM_001313913.2:c.1182T>C | NP_001300842.1:p.Gly394= |