Linked Data
ClinVar Variation Id:
1597835
ClinVar RCV Id:
RCV002129410
dbSNP Id:
rs778980650
ExAC:
15:91310126 A / G
gnomAD v2:
15-91310126-A-G
gnomAD v3:
15-90766896-A-G
gnomAD v4:
15-90766896-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.90766896A>G , CM000677.2:g.90766896A>G | GRCh38 |
| NC_000015.9:g.91310126A>G , CM000677.1:g.91310126A>G | GRCh37 |
| NC_000015.8:g.89111130A>G | NCBI36 |
| NG_007272.1:g.54525A>G , LRG_20:g.54525A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355112.8:c.2194-14A>G MANE Select | ENSP00000347232.3:n.2194-14A>G | |
| ENST00000648453.1:c.2194-14A>G | ENSP00000497646.1:n.2194-14A>G | |
| ENST00000680772.1:c.2194-14A>G | ENSP00000506117.1:n.2194-14A>G | |
| ENST00000681142.1:c.2194-14A>G | ENSP00000506682.1:n.2194-14A>G | |
| ENST00000355112.7:c.2194-14A>G | ENSP00000347232.3:n.2194-14A>G | |
| ENST00000559426.5:n.371-14A>G | ||
| ENST00000559724.5:c.*1118-14A>G | ENSP00000453359.1:n.*1118-14A>G | |
| ENST00000560136.5:n.220-14A>G | ||
| ENST00000560509.5:c.2194-14A>G | ENSP00000454158.1:n.2194-14A>G | |
| NM_000057.3:c.2194-14A>G | NP_000048.1:n.2194-14A>G | |
| NM_001287246.1:c.2194-14A>G | NP_001274175.1:n.2194-14A>G | |
| NM_001287247.1:c.2194-14A>G | NP_001274176.1:n.2194-14A>G | |
| NM_001287248.1:c.1069-14A>G | NP_001274177.1:n.1069-14A>G | |
| XM_006720632.2:c.232-14A>G | XP_006720695.1:n.232-14A>G | |
| XM_011521881.1:c.880-14A>G | XP_011520183.1:n.880-14A>G | |
| XM_011521882.1:c.2194-14A>G | XP_011520184.1:n.2194-14A>G | |
| XM_011521881.2:c.880-14A>G | XP_011520183.1:n.880-14A>G | |
| XM_011521882.3:c.2194-14A>G | XP_011520184.1:n.2194-14A>G | |
| NM_000057.4:c.2194-14A>G MANE Select | NP_000048.1:n.2194-14A>G | |
| NM_001287246.2:c.2194-14A>G | NP_001274175.1:n.2194-14A>G | |
| NM_001287247.2:c.2194-14A>G | NP_001274176.1:n.2194-14A>G | |
| NM_001287248.2:c.1069-14A>G | NP_001274177.1:n.1069-14A>G |