Linked Data
ClinVar Variation Id:
456159
ClinVar RCV Id:
RCV000558309
dbSNP Id:
rs1057517219
gnomAD v4:
9-95240745-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.95240745T>C , CM000671.2:g.95240745T>C | GRCh38 |
| NC_000009.11:g.98003027T>C , CM000671.1:g.98003027T>C | GRCh37 |
| NC_000009.10:g.97042848T>C | NCBI36 |
| NG_011707.1:g.81965A>G , LRG_497:g.81965A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696261.1:n.497-2A>G | ||
| ENST00000696262.1:c.251-2A>G | ENSP00000512510.1:n.251-2A>G | |
| ENST00000289081.8:c.251-2A>G MANE Select | ENSP00000289081.3:n.251-2A>G | |
| ENST00000375305.6:c.251-2A>G | ENSP00000364454.1:n.251-2A>G | |
| ENST00000490972.7:c.251-2A>G | ENSP00000479931.1:n.251-2A>G | |
| ENST00000636777.1:n.309-2A>G | ||
| ENST00000647778.1:c.251-2A>G | ENSP00000498125.1:n.251-2A>G | |
| ENST00000647882.1:c.251-2A>G | ENSP00000497025.1:n.251-2A>G | |
| ENST00000648415.1:n.1889-2A>G | ||
| ENST00000649334.1:c.251-2A>G | ENSP00000497735.1:n.251-2A>G | |
| ENST00000649519.1:c.251-2A>G | ENSP00000497630.1:n.251-2A>G | |
| ENST00000649872.1:c.251-2A>G | ENSP00000497195.1:n.251-2A>G | |
| ENST00000650176.1:n.431-2A>G | ||
| ENST00000289081.7:c.251-2A>G | ENSP00000289081.3:n.251-2A>G | |
| ENST00000375305.5:c.251-2A>G | ENSP00000364454.1:n.251-2A>G | |
| ENST00000433829.1:c.251-2A>G | ENSP00000406908.1:n.251-2A>G | |
| ENST00000474949.1:n.513-2A>G | ||
| ENST00000490972.6:c.251-2A>G | ENSP00000479931.1:n.251-2A>G | |
| NM_000136.2:c.251-2A>G , LRG_497t1:c.251-2A>G | NP_000127.2:n.251-2A>G | |
| NM_001243743.1:c.251-2A>G | NP_001230672.1:n.251-2A>G | |
| NM_001243744.1:c.251-2A>G | NP_001230673.1:n.251-2A>G | |
| XM_006717001.1:c.251-2A>G | XP_006717064.1:n.251-2A>G | |
| XM_006717002.2:c.251-2A>G | XP_006717065.1:n.251-2A>G | |
| XM_006717004.2:c.251-2A>G | XP_006717067.1:n.251-2A>G | |
| XM_011518365.1:c.251-2A>G | XP_011516667.1:n.251-2A>G | |
| XM_011518366.1:c.251-2A>G | XP_011516668.1:n.251-2A>G | |
| XM_011518367.1:c.-351-2A>G | XP_011516669.1:n.-351-2A>G | |
| XM_006717001.3:c.251-2A>G | XP_006717064.1:n.251-2A>G | |
| XM_006717002.4:c.251-2A>G | XP_006717065.1:n.251-2A>G | |
| XM_006717004.4:c.251-2A>G | XP_006717067.1:n.251-2A>G | |
| XM_011518365.3:c.251-2A>G | XP_011516667.1:n.251-2A>G | |
| XM_011518366.3:c.251-2A>G | XP_011516668.1:n.251-2A>G | |
| XM_011518367.2:c.-351-2A>G | XP_011516669.1:n.-351-2A>G | |
| XM_017014452.2:c.-351-2A>G | XP_016869941.1:n.-351-2A>G | |
| XM_017014453.1:c.-351-2A>G | XP_016869942.1:n.-351-2A>G | |
| XM_017014454.1:c.-351-2A>G | XP_016869943.1:n.-351-2A>G | |
| XM_024447451.1:c.251-2A>G | XP_024303219.1:n.251-2A>G | |
| NM_000136.3:c.251-2A>G MANE Select | NP_000127.2:n.251-2A>G | |
| NM_001243743.2:c.251-2A>G | NP_001230672.1:n.251-2A>G | |
| NM_001243744.2:c.251-2A>G | NP_001230673.1:n.251-2A>G |