Linked Data
ClinVar Variation Id:
859123
dbSNP Id:
rs1489553085
gnomAD v2:
11-67254552-C-T
gnomAD v4:
11-67487081-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67487081C>T , CM000673.2:g.67487081C>T | GRCh38 |
| NC_000011.9:g.67254552C>T , CM000673.1:g.67254552C>T | GRCh37 |
| NC_000011.8:g.67011128C>T | NCBI36 |
| NG_008969.1:g.9048C>T , LRG_460:g.9048C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525341.2:c.152C>T | ||
| ENST00000528641.7:c.175C>T | ENSP00000434982.3:p.Pro59Ser | |
| ENST00000529797.2:n.105C>T | ||
| ENST00000682324.1:c.175C>T | ENSP00000508017.1:p.Pro59Ser | |
| ENST00000682659.1:c.100-2957C>T | ENSP00000507351.1:n.100-2957C>T | |
| ENST00000682699.1:c.175C>T | ENSP00000507935.1:p.Pro59Ser | |
| ENST00000683237.1:c.175C>T | ENSP00000507343.1:p.Pro59Ser | |
| ENST00000683856.1:c.-3C>T | ENSP00000507979.1:n.-3C>T | |
| ENST00000684006.1:c.175C>T | ENSP00000507269.1:p.Pro59Ser | |
| ENST00000684657.1:c.100-2186C>T | ENSP00000507961.1:n.100-2186C>T | |
| ENST00000279146.8:c.175C>T MANE Select | ENSP00000279146.3:p.Pro59Ser | |
| ENST00000279146.7:c.175C>T | ENSP00000279146.3:p.Pro59Ser | |
| ENST00000528641.6:c.175C>T | ENSP00000434982.2:p.Pro59Ser | |
| ENST00000529797.1:n.285C>T | ||
| NM_001302959.1:c.-3C>T | NP_001289888.1:n.-3C>T | |
| NM_001302960.1:c.175C>T | NP_001289889.1:p.Pro59Ser | |
| NM_003977.3:c.175C>T | NP_003968.3:p.Pro59Ser | |
| XM_024448761.1:c.175C>T | XP_024304529.1:p.Pro59Ser | |
| NM_003977.4:c.175C>T MANE Select | NP_003968.3:p.Pro59Ser | |
| NM_001302960.2:c.175C>T | NP_001289889.1:p.Pro59Ser | |
| NM_001302959.2:c.-3C>T | NP_001289888.1:n.-3C>T |