Linked Data
ClinVar Variation Id:
233125
dbSNP Id:
rs777784520
gnomAD v2:
19-1218443-G-T
gnomAD v4:
19-1218444-G-T
COSMIC:
COSM21379
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1218444G>T , CM000681.2:g.1218444G>T | GRCh38 |
| NC_000019.9:g.1218443G>T , CM000681.1:g.1218443G>T | GRCh37 |
| NC_000019.8:g.1169443G>T | NCBI36 |
| NG_007460.2:g.34038G>T , LRG_319:g.34038G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000585465.3:c.318G>T | ENSP00000490268.2:p.Arg106= | |
| ENST00000585748.3:c.-55G>T | ENSP00000477641.2:n.-55G>T | |
| ENST00000585851.2:c.291-1929G>T | ENSP00000467912.2:n.291-1929G>T | |
| ENST00000326873.12:c.318G>T MANE Select | ENSP00000324856.6:p.Arg106= | |
| ENST00000652231.1:c.318G>T | ENSP00000498804.1:p.Arg106= | |
| ENST00000326873.11:c.318G>T | ENSP00000324856.6:p.Arg106= | |
| ENST00000585748.2:c.-55G>T | ENSP00000477641.1:n.-55G>T | |
| ENST00000585851.1:c.291-1929G>T | ENSP00000467912.1:n.291-1929G>T | |
| ENST00000586243.5:c.318G>T | ENSP00000467240.2:p.Arg106= | |
| ENST00000586358.5:n.141G>T | ||
| ENST00000589152.5:n.408G>T | ||
| ENST00000593219.5:c.*143G>T | ENSP00000466610.1:n.*143G>T | |
| NM_000455.4:c.318G>T , LRG_319t1:c.318G>T | NP_000446.1:p.Arg106= | |
| XM_005259617.1:c.318G>T | XP_005259674.1:p.Arg106= | |
| XM_005259618.3:c.318G>T | XP_005259675.1:p.Arg106= | |
| XM_011528209.1:c.96G>T | XP_011526511.1:p.Arg32= | |
| XR_936204.1:n.943G>T | ||
| XM_005259617.3:c.318G>T | XP_005259674.1:p.Arg106= | |
| XM_011528209.2:c.96G>T | XP_011526511.1:p.Arg32= | |
| XR_001753738.2:n.943G>T | ||
| XR_001753739.1:n.943G>T | ||
| XR_001753740.2:n.943G>T | ||
| NM_000455.5:c.318G>T MANE Select | NP_000446.1:p.Arg106= |