Linked Data
dbSNP Id:
rs765500776
ExAC:
X:138643667 A / G
gnomAD v2:
X-138643667-A-G
gnomAD v3:
X-139561508-A-G
gnomAD v4:
X-139561508-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.139561508A>G , CM000685.2:g.139561508A>G | GRCh38 |
| NC_000023.10:g.138643667A>G , CM000685.1:g.138643667A>G | GRCh37 |
| NC_000023.9:g.138471333A>G | NCBI36 |
| NG_007994.1:g.35773A>G , LRG_556:g.35773A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000218099.7:c.839-16A>G MANE Select | ENSP00000218099.2:n.839-16A>G | |
| ENST00000643157.1:n.1506-16A>G | ||
| ENST00000218099.6:c.839-16A>G | ENSP00000218099.2:n.839-16A>G | |
| ENST00000394090.2:c.725-16A>G | ENSP00000377650.2:n.725-16A>G | |
| NM_000133.3:c.839-16A>G , LRG_556t1:c.839-16A>G | NP_000124.1:n.839-16A>G | |
| NM_001313913.1:c.725-16A>G | NP_001300842.1:n.725-16A>G | |
| XM_005262397.3:c.710-16A>G | XP_005262454.1:n.710-16A>G | |
| XM_005262397.4:c.710-16A>G | XP_005262454.1:n.710-16A>G | |
| NM_000133.4:c.839-16A>G MANE Select | NP_000124.1:n.839-16A>G | |
| NM_001313913.2:c.725-16A>G | NP_001300842.1:n.725-16A>G |