Linked Data
ClinVar Variation Id:
542190
dbSNP Id:
rs201202020
ExAC:
14:58955474 T / G
gnomAD v2:
14-58955474-T-G
gnomAD v3:
14-58488756-T-G
gnomAD v4:
14-58488756-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.58488756T>G , CM000676.2:g.58488756T>G | GRCh38 |
| NC_000014.8:g.58955474T>G , CM000676.1:g.58955474T>G | GRCh37 |
| NC_000014.7:g.58025227T>G | NCBI36 |
| NG_051335.2:g.66372T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000619722.5:c.3408T>G | ENSP00000481936.1:p.Ser1136= | |
| ENST00000650845.1:n.4128T>G | ||
| ENST00000650904.1:c.3582T>G | ENSP00000498606.1:p.Ser1194= | |
| ENST00000651596.1:c.413T>G | ||
| ENST00000651759.1:c.2331T>G | ENSP00000498415.1:p.Ser777= | |
| ENST00000651852.1:c.1182T>G | ENSP00000498990.1:p.Ser394= | |
| ENST00000651937.1:c.*1866T>G | ENSP00000498785.1:n.*1866T>G | |
| ENST00000652326.2:c.3663T>G MANE Select | ENSP00000498929.1:p.Ser1221= | |
| ENST00000652414.1:c.1767T>G | ENSP00000498397.1:p.Ser589= | |
| ENST00000652732.1:c.*3148T>G | ENSP00000498799.1:n.*3148T>G | |
| ENST00000261244.9:c.3435T>G | ENSP00000261244.5:p.Ser1145= | |
| ENST00000354386.10:c.3822T>G | ENSP00000346359.6:p.Ser1274= | |
| ENST00000423743.7:c.3531T>G | ENSP00000399427.3:p.Ser1177= | |
| ENST00000538571.6:n.3253T>G | ||
| ENST00000556134.5:c.3531T>G | ENSP00000452351.2:p.Ser1177= | |
| ENST00000619416.4:c.3618T>G | ENSP00000478083.1:p.Ser1206= | |
| ENST00000619722.4:c.3408T>G | ENSP00000481936.1:p.Ser1136= | |
| NM_001244189.1:c.3822T>G | NP_001231118.1:p.Ser1274= | |
| NM_001244190.1:c.3618T>G | NP_001231119.1:p.Ser1206= | |
| NM_001244191.1:c.3408T>G | NP_001231120.1:p.Ser1136= | |
| NM_001244192.1:c.3531T>G | NP_001231121.1:p.Ser1177= | |
| NM_001244193.1:c.3243T>G | NP_001231122.1:p.Ser1081= | |
| NM_014749.3:c.3435T>G | NP_055564.3:p.Ser1145= | |
| NM_001329943.2:c.3663T>G | NP_001316872.1:p.Ser1221= | |
| NM_001329944.1:c.3663T>G | NP_001316873.1:p.Ser1221= | |
| NM_001329945.1:c.3408T>G | NP_001316874.1:p.Ser1136= | |
| NM_001329946.1:c.3663T>G | NP_001316875.1:p.Ser1221= | |
| NM_001329947.1:c.3663T>G | NP_001316876.1:p.Ser1221= | |
| NM_001364700.1:c.3408T>G | NP_001351629.1:p.Ser1136= | |
| NM_001364701.1:c.3408T>G | NP_001351630.1:p.Ser1136= | |
| NM_014749.4:c.3435T>G | NP_055564.3:p.Ser1145= | |
| XM_024449779.1:c.3786T>G | XP_024305547.1:p.Ser1262= | |
| XM_024449780.1:c.3687T>G | XP_024305548.1:p.Ser1229= | |
| XM_024449781.1:c.3786T>G | XP_024305549.1:p.Ser1262= | |
| XM_024449782.1:c.3432T>G | XP_024305550.1:p.Ser1144= | |
| XM_024449783.1:c.3432T>G | XP_024305551.1:p.Ser1144= | |
| XM_024449784.1:c.3432T>G | XP_024305552.1:p.Ser1144= | |
| XM_024449785.1:c.3408T>G | XP_024305553.1:p.Ser1136= | |
| XM_024449787.1:c.3267T>G | XP_024305555.1:p.Ser1089= | |
| XM_024449788.1:c.3243T>G | XP_024305556.1:p.Ser1081= | |
| XM_024449789.1:c.3243T>G | XP_024305557.1:p.Ser1081= | |
| XM_024449791.1:c.3687T>G | XP_024305559.1:p.Ser1229= | |
| NM_001244189.2:c.3822T>G | NP_001231118.1:p.Ser1274= | |
| NM_001244190.2:c.3618T>G | NP_001231119.1:p.Ser1206= | |
| NM_001244192.2:c.3531T>G | NP_001231121.1:p.Ser1177= | |
| NM_001329943.3:c.3663T>G MANE Select | NP_001316872.1:p.Ser1221= | |
| NM_001329944.2:c.3663T>G | NP_001316873.1:p.Ser1221= | |
| NM_001329945.2:c.3408T>G | NP_001316874.1:p.Ser1136= | |
| NM_001329946.2:c.3663T>G | NP_001316875.1:p.Ser1221= | |
| NM_001329947.2:c.3663T>G | NP_001316876.1:p.Ser1221= | |
| NM_001364701.2:c.3408T>G | NP_001351630.1:p.Ser1136= | |
| NM_014749.5:c.3435T>G | NP_055564.3:p.Ser1145= | |
| NM_001244191.2:c.3408T>G | NP_001231120.1:p.Ser1136= | |
| NM_001244193.2:c.3243T>G | NP_001231122.1:p.Ser1081= |