Linked Data
ClinVar Variation Id:
1992533
ClinVar RCV Id:
RCV002796008
dbSNP Id:
rs1481103115
gnomAD v2:
7-44684997-C-T
gnomAD v4:
7-44645398-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.44645398C>T , CM000669.2:g.44645398C>T | GRCh38 |
| NC_000007.13:g.44684997C>T , CM000669.1:g.44684997C>T | GRCh37 |
| NC_000007.12:g.44651522C>T | NCBI36 |
| NG_023260.1:g.43877C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000447398.6:c.294C>T | ENSP00000388183.1:p.Pro98= | |
| ENST00000222673.6:c.294C>T MANE Select | ENSP00000222673.5:p.Pro98= | |
| ENST00000222673.5:c.294C>T | ENSP00000222673.5:p.Pro98= | |
| ENST00000419661.5:c.294C>T | ENSP00000411830.1:p.Pro98= | |
| ENST00000439616.6:c.222+20833C>T | ENSP00000398576.2:n.222+20833C>T | |
| ENST00000443864.6:c.294C>T | ENSP00000388084.2:p.Pro98= | |
| ENST00000444676.5:c.294C>T | ENSP00000414662.1:p.Pro98= | |
| ENST00000447398.5:c.294C>T | ENSP00000388183.1:p.Pro98= | |
| ENST00000449767.5:c.294C>T | ENSP00000392878.1:p.Pro98= | |
| ENST00000631326.2:c.294C>T | ENSP00000486854.1:p.Pro98= | |
| NM_001003941.2:c.294C>T | NP_001003941.1:p.Pro98= | |
| NM_001165036.1:c.294C>T | NP_001158508.1:p.Pro98= | |
| NM_002541.3:c.294C>T | NP_002532.2:p.Pro98= | |
| XM_005249759.3:c.294C>T | XP_005249816.1:p.Pro98= | |
| XM_005249761.2:c.294C>T | XP_005249818.1:p.Pro98= | |
| XM_011515408.1:c.294C>T | XP_011513710.1:p.Pro98= | |
| NM_001363523.1:c.294C>T | NP_001350452.1:p.Pro98= | |
| XM_005249759.5:c.294C>T | XP_005249816.1:p.Pro98= | |
| XM_011515408.2:c.294C>T | XP_011513710.1:p.Pro98= | |
| NM_002541.4:c.294C>T MANE Select | NP_002532.2:p.Pro98= | |
| NM_001003941.3:c.294C>T | NP_001003941.1:p.Pro98= | |
| NM_001165036.2:c.294C>T | NP_001158508.1:p.Pro98= | |
| NM_001363523.2:c.294C>T | NP_001350452.1:p.Pro98= |