Linked Data
ClinVar Variation Id:
480512
dbSNP Id:
rs755838887
gnomAD v2:
17-56811546-C-G
gnomAD v4:
17-58734185-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58734185C>G , CM000679.2:g.58734185C>G | GRCh38 |
| NC_000017.10:g.56811546C>G , CM000679.1:g.56811546C>G | GRCh37 |
| NC_000017.9:g.54166545C>G | NCBI36 |
| NG_023199.1:g.46584C>G , LRG_314:g.46584C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461271.6:c.*1626C>G | ENSP00000464056.2:n.*1626C>G | |
| ENST00000697680.1:c.*2058C>G | ENSP00000513392.1:n.*2058C>G | |
| ENST00000697681.1:c.*2255C>G | ENSP00000513393.1:n.*2255C>G | |
| ENST00000697683.1:c.*2030C>G | ENSP00000513395.1:n.*2030C>G | |
| ENST00000697685.1:c.*1791C>G | ENSP00000513396.1:n.*1791C>G | |
| ENST00000697686.1:c.*4C>G | ENSP00000513397.1:n.*4C>G | |
| ENST00000697689.1:c.*1508C>G | ENSP00000513398.1:n.*1508C>G | |
| ENST00000697690.1:c.*54C>G | ENSP00000513399.1:n.*54C>G | |
| ENST00000697691.1:c.*1066C>G | ENSP00000513400.1:n.*1066C>G | |
| ENST00000697692.1:c.*1106C>G | ENSP00000513401.1:n.*1106C>G | |
| ENST00000697694.1:c.743C>G | ENSP00000513402.1:p.Thr248Ser | |
| ENST00000697695.1:n.1701C>G | ||
| ENST00000337432.9:c.1094C>G MANE Select | ENSP00000336701.4:p.Thr365Ser | |
| ENST00000337432.8:c.1094C>G | ENSP00000336701.4:p.Thr365Ser | |
| ENST00000413590.5:c.735C>G | ||
| ENST00000461706.1:n.281C>G | ||
| ENST00000475762.5:c.*1730C>G | ENSP00000432421.1:n.*1730C>G | |
| ENST00000482007.5:c.*522C>G | ENSP00000433332.1:n.*522C>G | |
| ENST00000487525.5:c.*670C>G | ENSP00000431637.1:n.*670C>G | |
| ENST00000578151.1:n.307C>G | ||
| ENST00000581221.5:n.609C>G | ||
| ENST00000584804.1:c.328C>G | ENSP00000463658.1:n.328C>G | |
| NM_058216.2:c.1094C>G | NP_478123.1:p.Thr365Ser | |
| NR_103872.1:n.998C>G | ||
| XM_006722001.2:c.1097C>G | XP_006722064.1:p.Thr366Ser | |
| XM_006722002.2:c.*4C>G | XP_006722065.1:n.*4C>G | |
| XM_006722004.2:c.746C>G | XP_006722067.1:p.Thr249Ser | |
| XM_006722005.2:c.746C>G | XP_006722068.1:p.Thr249Ser | |
| XM_011525092.1:c.746C>G | XP_011523394.1:p.Thr249Ser | |
| XM_011525093.1:c.746C>G | XP_011523395.1:p.Thr249Ser | |
| XM_011525094.1:c.746C>G | XP_011523396.1:p.Thr249Ser | |
| XR_934513.1:n.1312C>G | ||
| XR_934886.1:n.149+3886G>C | ||
| XM_006722001.4:c.1097C>G | XP_006722064.1:p.Thr366Ser | |
| XM_006722002.4:c.*4C>G | XP_006722065.1:n.*4C>G | |
| XM_006722004.3:c.746C>G | XP_006722067.1:p.Thr249Ser | |
| XM_006722005.3:c.746C>G | XP_006722068.1:p.Thr249Ser | |
| XM_011525092.2:c.746C>G | XP_011523394.1:p.Thr249Ser | |
| XM_011525093.2:c.746C>G | XP_011523395.1:p.Thr249Ser | |
| XM_011525094.2:c.746C>G | XP_011523396.1:p.Thr249Ser | |
| XM_017024914.1:c.743C>G | XP_016880403.1:p.Thr248Ser | |
| XM_017024915.1:c.743C>G | XP_016880404.1:p.Thr248Ser | |
| XM_017024916.1:c.743C>G | XP_016880405.1:p.Thr248Ser | |
| XM_017024917.1:c.743C>G | XP_016880406.1:p.Thr248Ser | |
| XM_017024918.2:c.743C>G | XP_016880407.1:p.Thr248Ser | |
| XM_017024919.1:c.*4C>G | XP_016880408.1:n.*4C>G | |
| XR_934513.3:n.1743C>G | ||
| XR_934886.2:n.149+3886G>C | ||
| NM_058216.3:c.1094C>G MANE Select | NP_478123.1:p.Thr365Ser | |
| NR_103872.2:n.969C>G |