Linked Data
ClinVar Variation Id:
281727
dbSNP Id:
rs138001923
ExAC:
17:78022564 A / G
gnomAD v2:
17-78022564-A-G
gnomAD v3:
17-80048765-A-G
gnomAD v4:
17-80048765-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80048765A>G , CM000679.2:g.80048765A>G | GRCh38 |
| NC_000017.10:g.78022564A>G , CM000679.1:g.78022564A>G | GRCh37 |
| NC_000017.9:g.75637159A>G | NCBI36 |
| NG_029761.1:g.17134A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397545.9:c.855+4A>G MANE Select | ENSP00000380679.4:n.855+4A>G | |
| ENST00000269318.9:c.855+4A>G | ENSP00000269318.5:n.855+4A>G | |
| ENST00000374876.4:c.855+4A>G | ENSP00000364010.4:n.855+4A>G | |
| ENST00000374877.7:c.855+4A>G | ENSP00000364011.3:n.855+4A>G | |
| ENST00000397545.8:c.855+4A>G | ENSP00000380679.4:n.855+4A>G | |
| ENST00000573474.5:c.309+4A>G | ||
| ENST00000574799.5:n.392+4A>G | ||
| NM_001243342.1:c.855+4A>G | NP_001230271.1:n.855+4A>G | |
| NM_017950.3:c.855+4A>G | NP_060420.2:n.855+4A>G | |
| XM_005257492.3:c.855+4A>G | XP_005257549.1:n.855+4A>G | |
| XM_011524963.1:c.765+4A>G | XP_011523265.1:n.765+4A>G | |
| XM_011524965.1:c.855+4A>G | XP_011523267.1:n.855+4A>G | |
| XR_934495.1:n.886+4A>G | ||
| NM_001330508.1:c.855+4A>G | NP_001317437.1:n.855+4A>G | |
| XM_011524963.3:c.765+4A>G | XP_011523265.1:n.765+4A>G | |
| XM_011524965.3:c.855+4A>G | XP_011523267.1:n.855+4A>G | |
| XM_017024807.1:c.855+4A>G | XP_016880296.1:n.855+4A>G | |
| XM_024450821.1:c.765+4A>G | XP_024306589.1:n.765+4A>G | |
| XR_001752550.2:n.886+4A>G | ||
| XR_934495.2:n.886+4A>G | ||
| NM_017950.4:c.855+4A>G MANE Select | NP_060420.2:n.855+4A>G | |
| NM_001330508.2:c.855+4A>G | NP_001317437.1:n.855+4A>G | |
| NM_001243342.2:c.855+4A>G | NP_001230271.1:n.855+4A>G |