Linked Data
ClinVar Variation Id:
305541
dbSNP Id:
rs554781314
ExAC:
11:66456660 G / A
gnomAD v2:
11-66456660-G-A
gnomAD v3:
11-66689189-G-A
gnomAD v4:
11-66689189-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.66689189G>A , CM000673.2:g.66689189G>A | GRCh38 |
| NC_000011.9:g.66456660G>A , CM000673.1:g.66456660G>A | GRCh37 |
| NC_000011.8:g.66213236G>A | NCBI36 |
| NG_016150.1:g.37211C>T | |
| NG_016150.2:g.45173C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309996.7:c.5950-9C>T | ENSP00000311489.2:n.5950-9C>T | |
| ENST00000611817.5:c.5950-9C>T | ENSP00000480692.2:n.5950-9C>T | |
| ENST00000617502.5:c.5971-9C>T | ENSP00000482000.2:n.5971-9C>T | |
| ENST00000647510.2:c.5950-9C>T | ENSP00000508362.1:n.5950-9C>T | |
| ENST00000533211.6:c.5950-9C>T MANE Select | ENSP00000432568.1:n.5950-9C>T | |
| ENST00000647510.1:n.6477-9C>T | ||
| ENST00000309996.6:c.5950-9C>T | ENSP00000311489.2:n.5950-9C>T | |
| ENST00000529997.5:c.5950-9C>T | ENSP00000433593.1:n.5950-9C>T | |
| ENST00000532902.1:n.460-9C>T | ||
| ENST00000533211.5:c.5950-9C>T | ENSP00000432568.1:n.5950-9C>T | |
| ENST00000611817.4:c.1855-528C>T | ENSP00000480692.1:n.1855-528C>T | |
| ENST00000617502.4:c.1851+162C>T | ENSP00000482000.1:n.1851+162C>T | |
| NM_006946.2:c.5950-9C>T | NP_008877.1:n.5950-9C>T | |
| XM_005274192.3:c.5950-9C>T | XP_005274249.1:n.5950-9C>T | |
| XM_005274193.3:c.5950-9C>T | XP_005274250.1:n.5950-9C>T | |
| XM_006718669.2:c.5971-9C>T | XP_006718732.1:n.5971-9C>T | |
| XM_006718671.2:c.5950-9C>T | XP_006718734.1:n.5950-9C>T | |
| NM_006946.3:c.5950-9C>T | NP_008877.1:n.5950-9C>T | |
| XM_005274192.4:c.5950-9C>T | XP_005274249.1:n.5950-9C>T | |
| XM_006718669.3:c.5971-9C>T | XP_006718732.1:n.5971-9C>T | |
| XM_006718671.4:c.5950-9C>T | XP_006718734.1:n.5950-9C>T | |
| XM_017018174.1:c.5950-9C>T | XP_016873663.1:n.5950-9C>T | |
| XM_017018175.2:c.5950-9C>T | XP_016873664.1:n.5950-9C>T | |
| XM_017018176.1:c.5950-9C>T | XP_016873665.1:n.5950-9C>T | |
| XM_017018177.2:c.5950-9C>T | XP_016873666.1:n.5950-9C>T | |
| XM_017018178.1:c.5950-9C>T | XP_016873667.1:n.5950-9C>T | |
| NM_006946.4:c.5950-9C>T MANE Select | NP_008877.2:n.5950-9C>T |