Linked Data
dbSNP Id:
rs1311764821
gnomAD v2:
3-193365011-T-C
gnomAD v3:
3-193647222-T-C
gnomAD v4:
3-193647222-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.193647222T>C , CM000665.2:g.193647222T>C | GRCh38 |
| NC_000003.11:g.193365011T>C , CM000665.1:g.193365011T>C | GRCh37 |
| NC_000003.10:g.194847705T>C | NCBI36 |
| NG_011605.1:g.59079T>C , LRG_337:g.59079T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361510.8:c.1870+42T>C MANE Select | ENSP00000355324.2:n.1870+42T>C | |
| ENST00000361828.7:c.1705+42T>C | ENSP00000354429.3:n.1705+42T>C | |
| ENST00000361908.8:c.1816+42T>C | ENSP00000354681.3:n.1816+42T>C | |
| ENST00000392436.7:c.1705+42T>C | ENSP00000376231.3:n.1705+42T>C | |
| ENST00000392437.6:c.1759+42T>C | ENSP00000376232.2:n.1759+42T>C | |
| ENST00000642289.1:c.1644+42T>C | ||
| ENST00000642445.1:c.1705+42T>C | ENSP00000495535.1:n.1705+42T>C | |
| ENST00000642593.1:c.1705+42T>C | ENSP00000494273.1:n.1705+42T>C | |
| ENST00000643329.1:c.1387+42T>C | ENSP00000493673.1:n.1387+42T>C | |
| ENST00000643737.1:c.*1786+42T>C | ENSP00000494210.1:n.*1786+42T>C | |
| ENST00000644595.1:c.1705+42T>C | ENSP00000494121.1:n.1705+42T>C | |
| ENST00000644629.1:c.1292+42T>C | ||
| ENST00000644841.1:c.*189+42T>C | ENSP00000493988.1:n.*189+42T>C | |
| ENST00000644959.1:c.1674+42T>C | ||
| ENST00000645553.1:c.1720+42T>C | ENSP00000494725.1:n.1720+42T>C | |
| ENST00000646085.1:c.*1183+42T>C | ENSP00000494509.1:n.*1183+42T>C | |
| ENST00000646277.1:c.*306+42T>C | ENSP00000495289.1:n.*306+42T>C | |
| ENST00000646544.1:c.693+42T>C | ||
| ENST00000646699.1:c.1644+42T>C | ||
| ENST00000646793.1:c.1597+42T>C | ENSP00000494512.1:n.1597+42T>C | |
| ENST00000361150.6:c.1708+42T>C | ENSP00000354781.2:n.1708+42T>C | |
| ENST00000361510.6:c.1870+42T>C | ENSP00000355324.2:n.1870+42T>C | |
| ENST00000361715.6:c.1762+42T>C | ENSP00000355311.2:n.1762+42T>C | |
| ENST00000361828.6:c.1759+42T>C | ENSP00000354429.2:n.1759+42T>C | |
| ENST00000361908.7:c.1816+42T>C | ENSP00000354681.3:n.1816+42T>C | |
| ENST00000392438.7:c.1705+42T>C | ENSP00000376233.3:n.1705+42T>C | |
| ENST00000483516.1:n.203+42T>C | ||
| NM_015560.2:c.1705+42T>C , LRG_337t1:c.1705+42T>C | NP_056375.2:n.1705+42T>C | |
| NM_130831.2:c.1597+42T>C | NP_570844.1:n.1597+42T>C | |
| NM_130832.2:c.1651+42T>C | NP_570845.1:n.1651+42T>C | |
| NM_130833.2:c.1708+42T>C | NP_570846.1:n.1708+42T>C | |
| NM_130834.2:c.1759+42T>C | NP_570847.2:n.1759+42T>C | |
| NM_130835.2:c.1762+42T>C | NP_570848.1:n.1762+42T>C | |
| NM_130836.2:c.1816+42T>C | NP_570849.2:n.1816+42T>C | |
| NM_130837.2:c.1870+42T>C , LRG_337t2:c.1870+42T>C | NP_570850.2:n.1870+42T>C | |
| XM_011512863.1:c.1870+42T>C | XP_011511165.1:n.1870+42T>C | |
| XM_011512864.1:c.1816+42T>C | XP_011511166.1:n.1816+42T>C | |
| XM_011512865.1:c.1759+42T>C | XP_011511167.1:n.1759+42T>C | |
| XM_011512866.1:c.1708+42T>C | XP_011511168.1:n.1708+42T>C | |
| XM_011512867.1:c.1705+42T>C | XP_011511169.1:n.1705+42T>C | |
| XM_011512868.1:c.1597+42T>C | XP_011511170.1:n.1597+42T>C | |
| XM_011512869.1:c.1870+42T>C | XP_011511171.1:n.1870+42T>C | |
| XR_924835.1:n.671A>G | ||
| NM_001354663.1:c.1336+42T>C | NP_001341592.1:n.1336+42T>C | |
| NM_001354664.1:c.1333+42T>C | NP_001341593.1:n.1333+42T>C | |
| XR_001740158.2:n.2099+42T>C | ||
| XR_001740159.2:n.1934+42T>C | ||
| XR_001741074.1:n.564A>G | ||
| XR_924835.2:n.689A>G | ||
| NM_001354663.2:c.1336+42T>C | NP_001341592.1:n.1336+42T>C | |
| NM_001354664.2:c.1333+42T>C | NP_001341593.1:n.1333+42T>C | |
| NM_130831.3:c.1597+42T>C | NP_570844.1:n.1597+42T>C | |
| NM_130832.3:c.1651+42T>C | NP_570845.1:n.1651+42T>C | |
| NM_130834.3:c.1759+42T>C | NP_570847.2:n.1759+42T>C | |
| NM_130836.3:c.1816+42T>C | NP_570849.2:n.1816+42T>C | |
| NM_015560.3:c.1705+42T>C | NP_056375.2:n.1705+42T>C | |
| NM_130833.3:c.1708+42T>C | NP_570846.1:n.1708+42T>C | |
| NM_130835.3:c.1762+42T>C | NP_570848.1:n.1762+42T>C | |
| NM_130837.3:c.1870+42T>C MANE Select | NP_570850.2:n.1870+42T>C |