Linked Data
ClinVar Variation Id:
851636
ClinVar RCV Id:
RCV001796843
dbSNP Id:
rs757635087
ExAC:
2:202074286 G / A
gnomAD v2:
2-202074286-G-A
gnomAD v3:
2-201209563-G-A
gnomAD v4:
2-201209563-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.201209563G>A , CM000664.2:g.201209563G>A | GRCh38 |
| NC_000002.11:g.202074286G>A , CM000664.1:g.202074286G>A | GRCh37 |
| NC_000002.10:g.201782531G>A | NCBI36 |
| NG_007265.1:g.31432G>A , LRG_33:g.31432G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313728.12:c.1214+1G>A | ENSP00000314599.7:n.1214+1G>A | |
| ENST00000346817.10:c.1286+1G>A | ENSP00000237865.7:n.1286+1G>A | |
| ENST00000492363.6:c.*501+1G>A | ENSP00000512459.1:n.*501+1G>A | |
| ENST00000696199.1:c.721+5797G>A | ENSP00000512481.1:n.721+5797G>A | |
| ENST00000286186.11:c.1415+1G>A MANE Select | ENSP00000286186.6:n.1415+1G>A | |
| ENST00000272879.9:c.1415+1G>A | ENSP00000272879.5:n.1415+1G>A | |
| ENST00000286186.10:c.1415+1G>A | ENSP00000286186.6:n.1415+1G>A | |
| ENST00000313728.11:c.1214+1G>A | ENSP00000314599.7:n.1214+1G>A | |
| ENST00000346817.9:c.1286+1G>A | ENSP00000237865.7:n.1286+1G>A | |
| ENST00000360132.7:c.*501+1G>A | ENSP00000353250.3:n.*501+1G>A | |
| ENST00000448480.1:c.1286+1G>A | ENSP00000396835.1:n.1286+1G>A | |
| ENST00000492363.5:n.1323+1G>A | ||
| NM_001206524.1:c.1214+1G>A | NP_001193453.1:n.1214+1G>A | |
| NM_001206542.1:c.1286+1G>A | NP_001193471.1:n.1286+1G>A | |
| NM_001230.4:c.1286+1G>A | NP_001221.2:n.1286+1G>A | |
| NM_032974.4:c.1415+1G>A | NP_116756.2:n.1415+1G>A | |
| NM_032976.3:c.*501+1G>A | NP_116758.1:n.*501+1G>A | |
| NM_032977.3:c.1415+1G>A , LRG_33t1:c.1415+1G>A | NP_116759.2:n.1415+1G>A | |
| XM_005246907.2:c.1412+1G>A | XP_005246964.1:n.1412+1G>A | |
| XM_006712796.2:c.665+1G>A | XP_006712859.1:n.665+1G>A | |
| XM_006712796.3:c.665+1G>A | XP_006712859.1:n.665+1G>A | |
| NM_001206524.2:c.1214+1G>A | NP_001193453.1:n.1214+1G>A | |
| NM_001206542.2:c.1286+1G>A | NP_001193471.1:n.1286+1G>A | |
| NM_001230.5:c.1286+1G>A | NP_001221.2:n.1286+1G>A | |
| NM_032974.5:c.1415+1G>A | NP_116756.2:n.1415+1G>A | |
| NM_032977.4:c.1415+1G>A MANE Select | NP_116759.2:n.1415+1G>A | |
| NM_032976.4:c.*501+1G>A | NP_116758.1:n.*501+1G>A |