Linked Data
dbSNP Id:
rs111576990
ExAC:
17:61574321 G / T
gnomAD v2:
17-61574321-G-T
gnomAD v3:
17-63496960-G-T
gnomAD v4:
17-63496960-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63496960G>T , CM000679.2:g.63496960G>T | GRCh38 |
| NC_000017.10:g.61574321G>T , CM000679.1:g.61574321G>T | GRCh37 |
| NC_000017.9:g.58928053G>T | NCBI36 |
| NG_011648.1:g.24888G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290866.10:c.3666G>T MANE Select | ENSP00000290866.4:p.Pro1222= | |
| ENST00000290863.10:c.1944G>T | ENSP00000290863.6:p.Pro648= | |
| ENST00000290866.9:c.3666G>T | ENSP00000290866.4:p.Pro1222= | |
| ENST00000413513.7:c.1821G>T | ENSP00000392247.3:p.Pro607= | |
| ENST00000428043.5:c.3666G>T | ENSP00000397593.2:p.Pro1222= | |
| ENST00000577418.5:n.676G>T | ||
| ENST00000577647.2:c.1944G>T | ENSP00000464149.1:p.Pro648= | |
| ENST00000578839.5:c.*1421G>T | ENSP00000462110.2:n.*1421G>T | |
| ENST00000579314.5:c.*1395G>T | ENSP00000462599.1:n.*1395G>T | |
| ENST00000579409.1:c.353G>T | ||
| ENST00000582244.1:n.540G>T | ||
| NM_000789.3:c.3666G>T | NP_000780.1:p.Pro1222= | |
| NM_001178057.1:c.1821G>T | NP_001171528.1:p.Pro607= | |
| NM_152830.2:c.1944G>T | NP_690043.1:p.Pro648= | |
| XM_005257110.1:c.3117G>T | XP_005257167.1:p.Pro1039= | |
| XM_006721737.2:c.2004G>T | XP_006721800.2:p.Pro668= | |
| XM_006721737.3:c.2004G>T | XP_006721800.2:p.Pro668= | |
| NM_000789.4:c.3666G>T MANE Select | NP_000780.1:p.Pro1222= | |
| NM_001178057.2:c.1821G>T | NP_001171528.1:p.Pro607= | |
| NM_152830.3:c.1944G>T | NP_690043.1:p.Pro648= | |
| NM_001382700.1:c.3099G>T | NP_001369629.1:p.Pro1033= | |
| NM_001382701.1:c.2814G>T | NP_001369630.1:p.Pro938= | |
| NM_001382702.1:c.1281G>T | NP_001369631.1:p.Pro427= | |
| NR_168483.1:n.2044G>T |