Linked Data
ClinVar Variation Id:
229705
dbSNP Id:
rs1554897280
gnomAD v4:
10-87925558-G-T
COSMIC:
COSM5976
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87925558G>T , CM000672.2:g.87925558G>T | GRCh38 |
| NC_000010.10:g.89685315G>T , CM000672.1:g.89685315G>T | GRCh37 |
| NC_000010.9:g.89675295G>T | NCBI36 |
| NG_007466.2:g.67120G>T , LRG_311:g.67120G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.209+1G>T | ENSP00000514759.2:n.209+1G>T | |
| ENST00000710265.1:c.209+1G>T | ENSP00000518161.1:n.209+1G>T | |
| ENST00000472832.3:c.209+1G>T | ENSP00000483066.2:n.209+1G>T | |
| ENST00000688158.2:n.944+1G>T | ||
| ENST00000688922.2:c.209+1G>T | ENSP00000508742.2:n.209+1G>T | |
| ENST00000700021.1:c.165-5488G>T | ENSP00000514757.1:n.165-5488G>T | |
| ENST00000700022.1:c.209+1G>T | ENSP00000514758.1:n.209+1G>T | |
| ENST00000700029.1:c.43+1G>T | ||
| ENST00000706954.1:c.209+1G>T | ENSP00000516674.1:n.209+1G>T | |
| ENST00000706955.1:c.*244+1G>T | ENSP00000516675.1:n.*244+1G>T | |
| ENST00000686459.1:c.209+1G>T | ENSP00000508909.1:n.209+1G>T | |
| ENST00000688158.1:c.*320+1G>T | ENSP00000509254.1:n.*320+1G>T | |
| ENST00000688308.1:c.209+1G>T | ENSP00000508752.1:n.209+1G>T | |
| ENST00000688922.1:c.78+1G>T | ||
| ENST00000693560.1:c.728+1G>T | ENSP00000509861.1:n.728+1G>T | |
| ENST00000371953.8:c.209+1G>T MANE Select | ENSP00000361021.3:n.209+1G>T | |
| ENST00000371953.7:c.209+1G>T | ENSP00000361021.3:n.209+1G>T | |
| ENST00000498703.1:n.35+1G>T | ||
| ENST00000610634.1:c.107+1G>T | ENSP00000477517.1:n.107+1G>T | |
| NM_000314.5:c.209+1G>T | NP_000305.3:n.209+1G>T | |
| NM_000314.6:c.209+1G>T | NP_000305.3:n.209+1G>T | |
| NM_001304717.2:c.728+1G>T | NP_001291646.2:n.728+1G>T | |
| NM_001304718.1:c.-541-5488G>T | NP_001291647.1:n.-541-5488G>T | |
| XM_006717926.2:c.165-5488G>T | XP_006717989.1:n.165-5488G>T | |
| XM_011539981.1:c.209+1G>T | XP_011538283.1:n.209+1G>T | |
| XM_011539982.1:c.113+1G>T | XP_011538284.1:n.113+1G>T | |
| XR_945789.1:n.921+1G>T | ||
| XR_945790.1:n.921+1G>T | ||
| XR_945791.1:n.921+1G>T | ||
| NM_000314.7:c.209+1G>T | NP_000305.3:n.209+1G>T | |
| NM_001304717.5:c.728+1G>T | NP_001291646.4:n.728+1G>T | |
| NM_001304718.2:c.-541-5488G>T | NP_001291647.1:n.-541-5488G>T | |
| NM_000314.8:c.209+1G>T MANE Select | NP_000305.3:n.209+1G>T |