Linked Data
dbSNP Id:
rs1290081597
gnomAD v2:
4-187207131-C-T
gnomAD v3:
4-186285977-C-T
gnomAD v4:
4-186285977-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186285977C>T , CM000666.2:g.186285977C>T | GRCh38 |
| NC_000004.11:g.187207131C>T , CM000666.1:g.187207131C>T | GRCh37 |
| NC_000004.10:g.187444125C>T | NCBI36 |
| NG_008051.1:g.25014C>T , LRG_583:g.25014C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000403665.7:c.1480+164C>T MANE Select | ENSP00000384957.2:n.1480+164C>T | |
| ENST00000264691.4:c.176+164C>T | ||
| ENST00000264692.8:c.1318+164C>T | ENSP00000264692.5:n.1318+164C>T | |
| ENST00000403665.6:c.1480+164C>T | ENSP00000384957.2:n.1480+164C>T | |
| NM_000128.3:c.1480+164C>T , LRG_583t1:c.1480+164C>T | NP_000119.1:n.1480+164C>T | |
| XM_005262821.2:c.1483+164C>T | XP_005262878.1:n.1483+164C>T | |
| XM_005262822.2:c.1483+164C>T | XP_005262879.1:n.1483+164C>T | |
| XM_005262823.2:c.1213+164C>T | XP_005262880.1:n.1213+164C>T | |
| XM_005262824.1:c.1483+164C>T | XP_005262881.1:n.1483+164C>T | |
| XM_006714137.1:c.1435+164C>T | XP_006714200.1:n.1435+164C>T | |
| XR_938706.1:n.1888+164C>T | ||
| XR_938707.1:n.1888+164C>T | ||
| XM_005262821.4:c.1483+164C>T | XP_005262878.1:n.1483+164C>T | |
| XM_005262822.4:c.1483+164C>T | XP_005262879.1:n.1483+164C>T | |
| XM_005262823.4:c.1213+164C>T | XP_005262880.1:n.1213+164C>T | |
| XM_006714137.3:c.1435+164C>T | XP_006714200.1:n.1435+164C>T | |
| XR_001741172.2:n.1954+164C>T | ||
| NM_000128.4:c.1480+164C>T MANE Select | NP_000119.1:n.1480+164C>T |