Linked Data
ClinVar Variation Id:
167461
dbSNP Id:
rs144331955
ExAC:
12:7351629 C / T
gnomAD v2:
12-7351629-C-T
gnomAD v3:
12-7199033-C-T
gnomAD v4:
12-7199033-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.7199033C>T , CM000674.2:g.7199033C>T | GRCh38 |
| NC_000012.11:g.7351629C>T , CM000674.1:g.7351629C>T | GRCh37 |
| NC_000012.10:g.7242896C>T | NCBI36 |
| NG_008448.1:g.14871C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000675855.1:c.471C>T MANE Select | ENSP00000502374.1:p.Ala157= | |
| ENST00000266563.9:c.471C>T | ENSP00000266563.5:p.Ala157= | |
| ENST00000266564.7:c.471C>T | ENSP00000266564.3:p.Ala157= | |
| ENST00000396637.7:c.516C>T | ENSP00000379877.3:p.Ala172= | |
| ENST00000412720.6:c.534C>T | ENSP00000391601.2:p.Ala178= | |
| ENST00000420616.6:c.471C>T | ENSP00000410159.2:p.Ala157= | |
| ENST00000434354.6:c.516C>T | ENSP00000407401.2:p.Ala172= | |
| ENST00000455147.6:c.471C>T | ENSP00000400647.2:p.Ala157= | |
| ENST00000536883.5:c.222C>T | ENSP00000441553.1:p.Ala74= | |
| ENST00000537873.5:c.449-2702C>T | ENSP00000437938.1:n.449-2702C>T | |
| ENST00000539304.1:n.152C>T | ||
| ENST00000542539.5:c.471C>T | ENSP00000439025.1:p.Ala157= | |
| ENST00000543974.5:c.222C>T | ENSP00000438772.1:p.Ala74= | |
| ENST00000545220.1:n.367-2718C>T | ||
| ENST00000545574.5:c.435C>T | ENSP00000443500.1:p.Ala145= | |
| ENST00000545845.1:c.222C>T | ENSP00000440711.1:p.Ala74= | |
| NM_000319.4:c.471C>T | NP_000310.2:p.Ala157= | |
| NM_001131023.1:c.516C>T | NP_001124495.1:p.Ala172= | |
| NM_001131024.1:c.471C>T | NP_001124496.1:p.Ala157= | |
| NM_001131025.1:c.471C>T | NP_001124497.1:p.Ala157= | |
| NM_001131026.1:c.471C>T | NP_001124498.1:p.Ala157= | |
| NM_001300789.1:c.534C>T | NP_001287718.1:p.Ala178= | |
| XM_005253455.1:c.534C>T | XP_005253512.1:p.Ala178= | |
| XM_011520793.1:c.579C>T | XP_011519095.1:p.Ala193= | |
| XM_011520794.1:c.579C>T | XP_011519096.1:p.Ala193= | |
| XM_011520795.1:c.516C>T | XP_011519097.1:p.Ala172= | |
| XM_011520796.1:c.516C>T | XP_011519098.1:p.Ala172= | |
| XM_011520797.1:c.471C>T | XP_011519099.1:p.Ala157= | |
| XM_011520798.1:c.471C>T | XP_011519100.1:p.Ala157= | |
| XM_011520799.1:c.471C>T | XP_011519101.1:p.Ala157= | |
| XM_011520800.1:c.471C>T | XP_011519102.1:p.Ala157= | |
| XM_011520801.1:c.579C>T | XP_011519103.1:p.Ala193= | |
| XM_011520802.1:c.222C>T | XP_011519104.1:p.Ala74= | |
| NM_001351124.1:c.471C>T | NP_001338053.1:p.Ala157= | |
| NM_001351126.1:c.471C>T | NP_001338055.1:p.Ala157= | |
| NM_001351127.1:c.471C>T | NP_001338056.1:p.Ala157= | |
| NM_001351128.1:c.471C>T | NP_001338057.1:p.Ala157= | |
| NM_001351130.1:c.471C>T | NP_001338059.1:p.Ala157= | |
| NM_001351131.1:c.471C>T | NP_001338060.1:p.Ala157= | |
| NM_001351132.1:c.471C>T | NP_001338061.1:p.Ala157= | |
| NM_001351133.1:c.471C>T | NP_001338062.1:p.Ala157= | |
| NM_001351134.1:c.471C>T | NP_001338063.1:p.Ala157= | |
| NM_001351135.1:c.579C>T | NP_001338064.1:p.Ala193= | |
| NM_001351136.1:c.471C>T | NP_001338065.1:p.Ala157= | |
| NM_001351137.1:c.534C>T | NP_001338066.1:p.Ala178= | |
| NM_001351138.1:c.516C>T | NP_001338067.1:p.Ala172= | |
| NM_001351139.1:c.471C>T | NP_001338068.1:p.Ala157= | |
| NM_001351140.1:c.471C>T | NP_001338069.1:p.Ala157= | |
| XM_011520793.2:c.579C>T | XP_011519095.1:p.Ala193= | |
| XM_011520802.2:c.222C>T | XP_011519104.1:p.Ala74= | |
| XM_017019744.1:c.915C>T | XP_016875233.1:p.Ala305= | |
| XM_017019745.1:c.915C>T | XP_016875234.1:p.Ala305= | |
| XM_017019746.1:c.915C>T | XP_016875235.1:p.Ala305= | |
| XM_017019747.1:c.915C>T | XP_016875236.1:p.Ala305= | |
| XM_017019748.1:c.516C>T | XP_016875237.1:p.Ala172= | |
| XM_017019749.1:c.471C>T | XP_016875238.1:p.Ala157= | |
| XM_017019750.1:c.471C>T | XP_016875239.1:p.Ala157= | |
| XR_001748833.1:n.957C>T | ||
| NM_000319.5:c.471C>T | NP_000310.2:p.Ala157= | |
| NM_001131023.2:c.516C>T | NP_001124495.1:p.Ala172= | |
| NM_001131024.2:c.471C>T | NP_001124496.1:p.Ala157= | |
| NM_001131025.2:c.471C>T | NP_001124497.1:p.Ala157= | |
| NM_001131026.2:c.471C>T | NP_001124498.1:p.Ala157= | |
| NM_001300789.3:c.471C>T | NP_001287718.2:p.Ala157= | |
| NM_001351124.3:c.471C>T | NP_001338053.1:p.Ala157= | |
| NM_001351126.2:c.471C>T | NP_001338055.1:p.Ala157= | |
| NM_001351127.2:c.471C>T | NP_001338056.1:p.Ala157= | |
| NM_001351128.2:c.471C>T | NP_001338057.1:p.Ala157= | |
| NM_001351130.3:c.471C>T | NP_001338059.1:p.Ala157= | |
| NM_001351131.2:c.471C>T | NP_001338060.1:p.Ala157= | |
| NM_001351132.2:c.471C>T MANE Select | NP_001338061.1:p.Ala157= | |
| NM_001351133.2:c.471C>T | NP_001338062.1:p.Ala157= | |
| NM_001351134.2:c.471C>T | NP_001338063.1:p.Ala157= | |
| NM_001351135.3:c.516C>T | NP_001338064.2:p.Ala172= | |
| NM_001351136.2:c.471C>T | NP_001338065.1:p.Ala157= | |
| NM_001351137.3:c.471C>T | NP_001338066.2:p.Ala157= | |
| NM_001351138.2:c.516C>T | NP_001338067.1:p.Ala172= | |
| NM_001351139.2:c.471C>T | NP_001338068.1:p.Ala157= | |
| NM_001351140.2:c.471C>T | NP_001338069.1:p.Ala157= | |
| NM_001374645.1:c.471C>T | NP_001361574.1:p.Ala157= | |
| NM_001374646.1:c.471C>T | NP_001361575.1:p.Ala157= | |
| NM_001374647.2:c.471C>T | NP_001361576.1:p.Ala157= | |
| NM_001374648.2:c.471C>T | NP_001361577.1:p.Ala157= | |
| NM_001374649.2:c.471C>T | NP_001361578.1:p.Ala157= |