Linked Data
ClinVar Variation Id:
552918
ClinVar RCV Id:
RCV000668268
dbSNP Id:
rs180177366
gnomAD v3:
8-99717374-G-T
gnomAD v4:
8-99717374-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.99717374G>T , CM000670.2:g.99717374G>T | GRCh38 |
| NC_000008.10:g.100729602G>T , CM000670.1:g.100729602G>T | GRCh37 |
| NC_000008.9:g.100798778G>T | NCBI36 |
| NG_007098.2:g.709109G>T , LRG_351:g.709109G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000682153.1:c.6732+1G>T | ENSP00000507923.1:n.6732+1G>T | |
| ENST00000682358.1:n.6802+1G>T | ||
| ENST00000683334.1:c.*2414+1G>T | ENSP00000507369.1:n.*2414+1G>T | |
| ENST00000357162.7:c.6657+1G>T MANE Select | ENSP00000349685.2:n.6657+1G>T | |
| ENST00000358544.7:c.6732+1G>T MANE Plus Clinical | ENSP00000351346.2:n.6732+1G>T | |
| ENST00000357162.6:c.6657+1G>T | ENSP00000349685.2:n.6657+1G>T | |
| ENST00000358544.6:c.6732+1G>T | ENSP00000351346.2:n.6732+1G>T | |
| NM_017890.4:c.6732+1G>T , LRG_351t1:c.6732+1G>T | NP_060360.3:n.6732+1G>T | |
| NM_152564.4:c.6657+1G>T , LRG_351t2:c.6657+1G>T | NP_689777.3:n.6657+1G>T | |
| XM_005250800.2:c.6732+1G>T | XP_005250857.1:n.6732+1G>T | |
| XM_005250801.3:c.6732+1G>T | XP_005250858.1:n.6732+1G>T | |
| XM_011516848.1:c.6729+1G>T | XP_011515150.1:n.6729+1G>T | |
| XM_011516849.1:c.6654+1G>T | XP_011515151.1:n.6654+1G>T | |
| XM_011516850.1:c.6354+1G>T | XP_011515152.1:n.6354+1G>T | |
| XM_011516851.1:c.3618+1G>T | XP_011515153.1:n.3618+1G>T | |
| XM_011516852.1:c.3618+1G>T | XP_011515154.1:n.3618+1G>T | |
| XM_011516853.1:c.6732+1G>T | XP_011515155.1:n.6732+1G>T | |
| XM_011516854.1:c.2511+1G>T | XP_011515156.1:n.2511+1G>T | |
| XM_005250800.3:c.6732+1G>T | XP_005250857.1:n.6732+1G>T | |
| XM_005250801.5:c.6732+1G>T | XP_005250858.1:n.6732+1G>T | |
| XM_011516848.2:c.6729+1G>T | XP_011515150.1:n.6729+1G>T | |
| XM_011516849.2:c.6654+1G>T | XP_011515151.1:n.6654+1G>T | |
| XM_011516850.2:c.6354+1G>T | XP_011515152.1:n.6354+1G>T | |
| XM_011516851.2:c.3618+1G>T | XP_011515153.1:n.3618+1G>T | |
| XM_011516852.2:c.3618+1G>T | XP_011515154.1:n.3618+1G>T | |
| XM_011516853.2:c.6732+1G>T | XP_011515155.1:n.6732+1G>T | |
| XM_011516854.2:c.2511+1G>T | XP_011515156.1:n.2511+1G>T | |
| XM_017013109.1:c.6537+1G>T | XP_016868598.1:n.6537+1G>T | |
| XM_017013111.1:c.3618+1G>T | XP_016868600.1:n.3618+1G>T | |
| XM_017013112.1:c.2289+1G>T | XP_016868601.1:n.2289+1G>T | |
| XM_024447074.1:c.5517+1G>T | XP_024302842.1:n.5517+1G>T | |
| NM_017890.5:c.6732+1G>T MANE Plus Clinical | NP_060360.3:n.6732+1G>T | |
| NM_152564.5:c.6657+1G>T MANE Select | NP_689777.3:n.6657+1G>T |