Linked Data
ClinVar Variation Id:
1144602
ClinVar RCV Id:
RCV001483141
dbSNP Id:
rs2148367626
MyVariant Identifiers:
chrX:g.138643705A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.139561546A>T , CM000685.2:g.139561546A>T | GRCh38 |
| NC_000023.10:g.138643705A>T , CM000685.1:g.138643705A>T | GRCh37 |
| NC_000023.9:g.138471371A>T | NCBI36 |
| NG_007994.1:g.35811A>T , LRG_556:g.35811A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218099.7:c.861A>T MANE Select | ENSP00000218099.2:p.Thr287= | |
| ENST00000643157.1:n.1528A>T | ||
| ENST00000218099.6:c.861A>T | ENSP00000218099.2:p.Thr287= | |
| ENST00000394090.2:c.747A>T | ENSP00000377650.2:p.Thr249= | |
| NM_000133.3:c.861A>T , LRG_556t1:c.861A>T | NP_000124.1:p.Thr287= | |
| NM_001313913.1:c.747A>T | NP_001300842.1:p.Thr249= | |
| XM_005262397.3:c.732A>T | XP_005262454.1:p.Thr244= | |
| XM_005262397.4:c.732A>T | XP_005262454.1:p.Thr244= | |
| NM_000133.4:c.861A>T MANE Select | NP_000124.1:p.Thr287= | |
| NM_001313913.2:c.747A>T | NP_001300842.1:p.Thr249= |