Linked Data
dbSNP Id:
rs1734080786
gnomAD v4:
3-193643435-T-G
MyVariant Identifiers:
chr3:g.193361224T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.193643435T>G , CM000665.2:g.193643435T>G | GRCh38 |
| NC_000003.11:g.193361224T>G , CM000665.1:g.193361224T>G | GRCh37 |
| NC_000003.10:g.194843918T>G | NCBI36 |
| NG_011605.1:g.55292T>G , LRG_337:g.55292T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361510.8:c.1368T>G MANE Select | ENSP00000355324.2:p.Gly456= | |
| ENST00000361828.7:c.1203T>G | ENSP00000354429.3:p.Gly401= | |
| ENST00000361908.8:c.1314T>G | ENSP00000354681.3:p.Gly438= | |
| ENST00000392436.7:c.1203T>G | ENSP00000376231.3:p.Gly401= | |
| ENST00000392437.6:c.1257T>G | ENSP00000376232.2:p.Gly419= | |
| ENST00000642289.1:c.1142T>G | ||
| ENST00000642445.1:c.1203T>G | ENSP00000495535.1:p.Gly401= | |
| ENST00000642593.1:c.1203T>G | ENSP00000494273.1:p.Gly401= | |
| ENST00000643329.1:c.885T>G | ENSP00000493673.1:p.Gly295= | |
| ENST00000643737.1:c.*1284T>G | ENSP00000494210.1:n.*1284T>G | |
| ENST00000644595.1:c.1203T>G | ENSP00000494121.1:p.Gly401= | |
| ENST00000644629.1:c.863T>G | ||
| ENST00000644841.1:c.831T>G | ENSP00000493988.1:p.Gly277= | |
| ENST00000644959.1:c.1172T>G | ||
| ENST00000645553.1:c.1218T>G | ENSP00000494725.1:p.Gly406= | |
| ENST00000646085.1:c.*681T>G | ENSP00000494509.1:n.*681T>G | |
| ENST00000646277.1:c.1368T>G | ENSP00000495289.1:p.Gly456= | |
| ENST00000646544.1:c.191T>G | ||
| ENST00000646699.1:c.1142T>G | ||
| ENST00000646793.1:c.1095T>G | ENSP00000494512.1:p.Gly365= | |
| ENST00000361150.6:c.1206T>G | ENSP00000354781.2:p.Gly402= | |
| ENST00000361510.6:c.1368T>G | ENSP00000355324.2:p.Gly456= | |
| ENST00000361715.6:c.1260T>G | ENSP00000355311.2:p.Gly420= | |
| ENST00000361828.6:c.1257T>G | ENSP00000354429.2:p.Gly419= | |
| ENST00000361908.7:c.1314T>G | ENSP00000354681.3:p.Gly438= | |
| ENST00000392438.7:c.1203T>G | ENSP00000376233.3:p.Gly401= | |
| ENST00000475899.1:n.399T>G | ||
| NM_015560.2:c.1203T>G , LRG_337t1:c.1203T>G | NP_056375.2:p.Gly401= | |
| NM_130831.2:c.1095T>G | NP_570844.1:p.Gly365= | |
| NM_130832.2:c.1149T>G | NP_570845.1:p.Gly383= | |
| NM_130833.2:c.1206T>G | NP_570846.1:p.Gly402= | |
| NM_130834.2:c.1257T>G | NP_570847.2:p.Gly419= | |
| NM_130835.2:c.1260T>G | NP_570848.1:p.Gly420= | |
| NM_130836.2:c.1314T>G | NP_570849.2:p.Gly438= | |
| NM_130837.2:c.1368T>G , LRG_337t2:c.1368T>G | NP_570850.2:p.Gly456= | |
| XM_011512863.1:c.1368T>G | XP_011511165.1:p.Gly456= | |
| XM_011512864.1:c.1314T>G | XP_011511166.1:p.Gly438= | |
| XM_011512865.1:c.1257T>G | XP_011511167.1:p.Gly419= | |
| XM_011512866.1:c.1206T>G | XP_011511168.1:p.Gly402= | |
| XM_011512867.1:c.1203T>G | XP_011511169.1:p.Gly401= | |
| XM_011512868.1:c.1095T>G | XP_011511170.1:p.Gly365= | |
| XM_011512869.1:c.1368T>G | XP_011511171.1:p.Gly456= | |
| NM_001354663.1:c.834T>G | NP_001341592.1:p.Gly278= | |
| NM_001354664.1:c.831T>G | NP_001341593.1:p.Gly277= | |
| XR_001740158.2:n.1597T>G | ||
| XR_001740159.2:n.1432T>G | ||
| NM_001354663.2:c.834T>G | NP_001341592.1:p.Gly278= | |
| NM_001354664.2:c.831T>G | NP_001341593.1:p.Gly277= | |
| NM_130831.3:c.1095T>G | NP_570844.1:p.Gly365= | |
| NM_130832.3:c.1149T>G | NP_570845.1:p.Gly383= | |
| NM_130834.3:c.1257T>G | NP_570847.2:p.Gly419= | |
| NM_130836.3:c.1314T>G | NP_570849.2:p.Gly438= | |
| NM_015560.3:c.1203T>G | NP_056375.2:p.Gly401= | |
| NM_130833.3:c.1206T>G | NP_570846.1:p.Gly402= | |
| NM_130835.3:c.1260T>G | NP_570848.1:p.Gly420= | |
| NM_130837.3:c.1368T>G MANE Select | NP_570850.2:p.Gly456= |