Linked Data
dbSNP Id:
rs940333309
gnomAD v3:
8-143817657-G-C
gnomAD v4:
8-143817657-G-C
MyVariant Identifiers:
chr8:g.143817657G>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.143817657G>C , CM000670.2:g.143817657G>C | GRCh38 |
| NC_000008.9:g.144971815G>C | NCBI36 |
| NG_030583.1:g.2723C>G | |
| NG_033879.1:g.16730C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000524570.6:n.1641C>G | ||
| ENST00000526151.6:n.2998C>G | ||
| ENST00000526459.6:c.889C>G | ENSP00000432610.2:p.Pro297Ala | |
| ENST00000527744.6:c.940C>G | ENSP00000436131.2:p.Pro314Ala | |
| ENST00000531951.6:c.814C>G | ENSP00000515500.1:p.Pro272Ala | |
| ENST00000532127.6:c.*788C>G | ENSP00000515484.1:n.*788C>G | |
| ENST00000533162.2:c.1054C>G | ENSP00000433403.2:p.Pro352Ala | |
| ENST00000533362.2:c.1018C>G | ENSP00000515502.1:p.Pro340Ala | |
| ENST00000703744.1:n.1654C>G | ||
| ENST00000703803.1:n.1208C>G | ||
| ENST00000703846.1:c.814C>G | ENSP00000515498.1:p.Pro272Ala | |
| ENST00000703847.1:c.1054C>G | ENSP00000515499.1:p.Pro352Ala | |
| ENST00000703848.1:n.974C>G | ||
| ENST00000703849.1:c.814C>G | ENSP00000515501.1:p.Pro272Ala | |
| ENST00000703850.1:c.1018C>G | ENSP00000515503.1:p.Pro340Ala | |
| ENST00000703851.1:n.863C>G | ||
| ENST00000703866.1:c.943C>G | ENSP00000515511.1:p.Pro315Ala | |
| ENST00000526683.6:c.943C>G MANE Select | ENSP00000434359.1:p.Pro315Ala | |
| ENST00000313352.11:c.763C>G | ENSP00000322016.7:p.Pro255Ala | |
| ENST00000349157.10:c.892C>G | ENSP00000322036.7:p.Pro298Ala | |
| ENST00000453551.6:c.814C>G | ENSP00000402953.2:p.Pro272Ala | |
| ENST00000456095.6:c.856C>G | ENSP00000395417.2:p.Pro286Ala | |
| ENST00000524570.5:n.1629C>G | ||
| ENST00000526459.5:c.889C>G | ENSP00000432610.1:p.Pro297Ala | |
| ENST00000526683.5:c.943C>G | ENSP00000434359.1:p.Pro315Ala | |
| ENST00000527197.5:c.805C>G | ENSP00000431960.1:p.Pro269Ala | |
| ENST00000527744.5:c.936C>G | ||
| ENST00000532884.1:c.552C>G | ||
| NM_001136033.2:c.814C>G | NP_001129505.1:p.Pro272Ala | |
| NM_001271096.1:c.889C>G | NP_001258025.1:p.Pro297Ala | |
| NM_001271097.1:c.805C>G | NP_001258026.1:p.Pro269Ala | |
| NM_001271098.1:c.940C>G | NP_001258027.1:p.Pro314Ala | |
| NM_001271099.1:c.856C>G | NP_001258028.1:p.Pro286Ala | |
| NM_001271100.1:c.763C>G | NP_001258029.1:p.Pro255Ala | |
| NM_014281.4:c.892C>G | NP_055096.2:p.Pro298Ala | |
| NM_078480.2:c.943C>G | NP_510965.1:p.Pro315Ala | |
| XM_011516929.1:c.1054C>G | XP_011515231.1:p.Pro352Ala | |
| XM_011516930.1:c.1003C>G | XP_011515232.1:p.Pro335Ala | |
| NM_001362895.1:c.1054C>G | NP_001349824.1:p.Pro352Ala | |
| NM_001362896.1:c.1054C>G | NP_001349825.1:p.Pro352Ala | |
| NM_001362897.1:c.1003C>G | NP_001349826.1:p.Pro335Ala | |
| XM_017013234.1:c.1054C>G | XP_016868723.1:p.Pro352Ala | |
| XM_017013235.1:c.1018C>G | XP_016868724.1:p.Pro340Ala | |
| XM_017013236.1:c.1003C>G | XP_016868725.1:p.Pro335Ala | |
| XM_017013239.1:c.814C>G | XP_016868728.1:p.Pro272Ala | |
| XM_017013240.1:c.763C>G | XP_016868729.1:p.Pro255Ala | |
| NM_001136033.3:c.814C>G | NP_001129505.1:p.Pro272Ala | |
| NM_001271096.2:c.889C>G | NP_001258025.1:p.Pro297Ala | |
| NM_001271097.2:c.805C>G | NP_001258026.1:p.Pro269Ala | |
| NM_001271098.2:c.940C>G | NP_001258027.1:p.Pro314Ala | |
| NM_001271099.2:c.856C>G | NP_001258028.1:p.Pro286Ala | |
| NM_001271100.2:c.763C>G | NP_001258029.1:p.Pro255Ala | |
| NM_001362895.2:c.1054C>G | NP_001349824.1:p.Pro352Ala | |
| NM_001362896.2:c.1054C>G | NP_001349825.1:p.Pro352Ala | |
| NM_001362897.2:c.1003C>G | NP_001349826.1:p.Pro335Ala | |
| NM_014281.5:c.892C>G | NP_055096.2:p.Pro298Ala | |
| NM_078480.3:c.943C>G MANE Select | NP_510965.1:p.Pro315Ala |