Linked Data
ClinVar Variation Id:
187748
dbSNP Id:
rs201235884
ExAC:
17:56801441 T / C
gnomAD v2:
17-56801441-T-C
gnomAD v3:
17-58724080-T-C
gnomAD v4:
17-58724080-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58724080T>C , CM000679.2:g.58724080T>C | GRCh38 |
| NC_000017.10:g.56801441T>C , CM000679.1:g.56801441T>C | GRCh37 |
| NC_000017.9:g.54156440T>C | NCBI36 |
| NG_023199.1:g.36479T>C , LRG_314:g.36479T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461271.6:c.594T>C | ENSP00000464056.2:p.Phe198= | |
| ENST00000697680.1:c.*1909T>C | ENSP00000513392.1:n.*1909T>C | |
| ENST00000697681.1:c.*2106T>C | ENSP00000513393.1:n.*2106T>C | |
| ENST00000697683.1:c.*1809T>C | ENSP00000513395.1:n.*1809T>C | |
| ENST00000697684.1:n.1005T>C | ||
| ENST00000697685.1:c.*1642T>C | ENSP00000513396.1:n.*1642T>C | |
| ENST00000697686.1:c.594T>C | ENSP00000513397.1:p.Phe198= | |
| ENST00000697687.1:n.824T>C | ||
| ENST00000697688.1:n.991T>C | ||
| ENST00000697689.1:c.*1440+3268T>C | ENSP00000513398.1:n.*1440+3268T>C | |
| ENST00000697690.1:c.904+3268T>C | ENSP00000513399.1:n.904+3268T>C | |
| ENST00000697691.1:c.*917T>C | ENSP00000513400.1:n.*917T>C | |
| ENST00000697692.1:c.*957T>C | ENSP00000513401.1:n.*957T>C | |
| ENST00000697694.1:c.594T>C | ENSP00000513402.1:p.Phe198= | |
| ENST00000697695.1:n.1552T>C | ||
| ENST00000337432.9:c.945T>C MANE Select | ENSP00000336701.4:p.Phe315= | |
| ENST00000337432.8:c.945T>C | ENSP00000336701.4:p.Phe315= | |
| ENST00000413590.5:c.583T>C | ||
| ENST00000475762.5:c.*1581T>C | ENSP00000432421.1:n.*1581T>C | |
| ENST00000482007.5:c.*373T>C | ENSP00000433332.1:n.*373T>C | |
| ENST00000487525.5:c.*518T>C | ENSP00000431637.1:n.*518T>C | |
| ENST00000578151.1:n.239+3268T>C | ||
| ENST00000581221.5:n.460T>C | ||
| ENST00000583539.5:c.945T>C | ENSP00000463121.1:p.Phe315= | |
| ENST00000584617.5:c.667T>C | ||
| ENST00000584804.1:c.199+3268T>C | ENSP00000463658.1:n.199+3268T>C | |
| NM_058216.2:c.945T>C | NP_478123.1:p.Phe315= | |
| NR_103872.1:n.849T>C | ||
| XM_006722001.2:c.945T>C | XP_006722064.1:p.Phe315= | |
| XM_006722002.2:c.904+3268T>C | XP_006722065.1:n.904+3268T>C | |
| XM_006722004.2:c.594T>C | XP_006722067.1:p.Phe198= | |
| XM_006722005.2:c.594T>C | XP_006722068.1:p.Phe198= | |
| XM_011525092.1:c.594T>C | XP_011523394.1:p.Phe198= | |
| XM_011525093.1:c.594T>C | XP_011523395.1:p.Phe198= | |
| XM_011525094.1:c.594T>C | XP_011523396.1:p.Phe198= | |
| XR_934513.1:n.1163T>C | ||
| XR_934514.1:n.1163T>C | ||
| XM_006722001.4:c.945T>C | XP_006722064.1:p.Phe315= | |
| XM_006722002.4:c.904+3268T>C | XP_006722065.1:n.904+3268T>C | |
| XM_006722004.3:c.594T>C | XP_006722067.1:p.Phe198= | |
| XM_006722005.3:c.594T>C | XP_006722068.1:p.Phe198= | |
| XM_011525092.2:c.594T>C | XP_011523394.1:p.Phe198= | |
| XM_011525093.2:c.594T>C | XP_011523395.1:p.Phe198= | |
| XM_011525094.2:c.594T>C | XP_011523396.1:p.Phe198= | |
| XM_017024914.1:c.594T>C | XP_016880403.1:p.Phe198= | |
| XM_017024915.1:c.594T>C | XP_016880404.1:p.Phe198= | |
| XM_017024916.1:c.594T>C | XP_016880405.1:p.Phe198= | |
| XM_017024917.1:c.594T>C | XP_016880406.1:p.Phe198= | |
| XM_017024918.2:c.594T>C | XP_016880407.1:p.Phe198= | |
| XM_017024919.1:c.553+3268T>C | XP_016880408.1:n.553+3268T>C | |
| XR_934513.3:n.1594T>C | ||
| XR_934514.3:n.1594T>C | ||
| NM_058216.3:c.945T>C MANE Select | NP_478123.1:p.Phe315= | |
| NR_103872.2:n.820T>C |