Linked Data
ClinVar Variation Id:
449063
dbSNP Id:
rs1044486319
gnomAD v3:
3-37050601-T-C
gnomAD v4:
3-37050601-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.37050601T>C , CM000665.2:g.37050601T>C | GRCh38 |
| NC_000003.11:g.37092092T>C , CM000665.1:g.37092092T>C | GRCh37 |
| NC_000003.10:g.37067096T>C | NCBI36 |
| NG_007109.2:g.62252T>C , LRG_216:g.62252T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000413740.2:c.1783T>C | ENSP00000416476.2:p.Ser595Pro | |
| ENST00000429117.6:c.1925T>C | ENSP00000407019.2:p.Ile642Thr | |
| ENST00000456676.7:c.2012T>C | ENSP00000416687.3:p.Ile671Thr | |
| ENST00000492474.6:c.1496T>C | ENSP00000518393.1:p.Ile499Thr | |
| ENST00000616768.6:c.2126T>C | ENSP00000480669.3:p.Ile709Thr | |
| ENST00000673673.2:c.2054T>C | ENSP00000500979.2:p.Ile685Thr | |
| ENST00000231790.8:c.2219T>C MANE Select | ENSP00000231790.3:p.Ile740Thr | |
| ENST00000413212.2:c.*1137T>C | ENSP00000400844.2:n.*1137T>C | |
| ENST00000432299.6:c.*2051T>C | ENSP00000416783.1:n.*2051T>C | |
| ENST00000447829.6:c.*1330T>C | ENSP00000399329.2:n.*1330T>C | |
| ENST00000539477.6:c.1496T>C | ENSP00000443665.1:p.Ile499Thr | |
| ENST00000616768.5:c.1163T>C | ENSP00000480669.2:p.Ile388Thr | |
| ENST00000673673.1:c.2007T>C | ||
| ENST00000673741.1:n.1253T>C | ||
| ENST00000673889.1:n.1601T>C | ||
| ENST00000673897.1:c.*2011T>C | ENSP00000501109.1:n.*2011T>C | |
| ENST00000673899.1:c.1487T>C | ENSP00000501030.1:p.Ile496Thr | |
| ENST00000673947.1:c.*2359T>C | ENSP00000501304.1:n.*2359T>C | |
| ENST00000673972.1:c.*2097T>C | ENSP00000501281.1:n.*2097T>C | |
| ENST00000674019.1:c.1496T>C | ENSP00000501081.1:p.Ile499Thr | |
| ENST00000674111.1:c.*448T>C | ENSP00000501162.1:n.*448T>C | |
| ENST00000674125.1:n.930T>C | ||
| ENST00000231790.6:c.2219T>C | ENSP00000231790.2:p.Ile740Thr | |
| ENST00000435176.5:c.1925T>C | ENSP00000402564.1:p.Ile642Thr | |
| ENST00000455445.6:c.1496T>C | ENSP00000398272.2:p.Ile499Thr | |
| ENST00000456676.6:c.1987T>C | ||
| ENST00000458205.6:c.1496T>C | ENSP00000402667.2:p.Ile499Thr | |
| ENST00000536378.5:c.1496T>C | ENSP00000444286.2:p.Ile499Thr | |
| ENST00000539477.5:c.1496T>C | ENSP00000443665.1:p.Ile499Thr | |
| NM_000249.3:c.2219T>C , LRG_216t1:c.2219T>C | NP_000240.1:p.Ile740Thr | |
| NM_001167617.1:c.1925T>C | NP_001161089.1:p.Ile642Thr | |
| NM_001167618.1:c.1496T>C | NP_001161090.1:p.Ile499Thr | |
| NM_001167619.1:c.1496T>C | NP_001161091.1:p.Ile499Thr | |
| NM_001258271.1:c.2012T>C | NP_001245200.1:p.Ile671Thr | |
| NM_001258273.1:c.1496T>C | NP_001245202.1:p.Ile499Thr | |
| NM_001258274.1:c.1496T>C | NP_001245203.1:p.Ile499Thr | |
| XM_005265161.1:c.2012T>C | XP_005265218.1:p.Ile671Thr | |
| XM_005265163.1:c.1496T>C | XP_005265220.1:p.Ile499Thr | |
| XM_005265164.1:c.1496T>C | XP_005265221.1:p.Ile499Thr | |
| XM_005265166.1:c.1196T>C | XP_005265223.1:p.Ile399Thr | |
| XM_011533727.1:c.1145T>C | XP_011532029.1:p.Ile382Thr | |
| NM_001167617.2:c.1925T>C | NP_001161089.1:p.Ile642Thr | |
| NM_001167618.2:c.1496T>C | NP_001161090.1:p.Ile499Thr | |
| NM_001167619.2:c.1496T>C | NP_001161091.1:p.Ile499Thr | |
| NM_001258274.2:c.1496T>C | NP_001245203.1:p.Ile499Thr | |
| NM_001354615.1:c.1496T>C | NP_001341544.1:p.Ile499Thr | |
| NM_001354616.1:c.1496T>C | NP_001341545.1:p.Ile499Thr | |
| NM_001354617.1:c.1496T>C | NP_001341546.1:p.Ile499Thr | |
| NM_001354618.1:c.1496T>C | NP_001341547.1:p.Ile499Thr | |
| NM_001354619.1:c.1496T>C | NP_001341548.1:p.Ile499Thr | |
| NM_001354620.1:c.1925T>C | NP_001341549.1:p.Ile642Thr | |
| NM_001354621.1:c.1196T>C | NP_001341550.1:p.Ile399Thr | |
| NM_001354622.1:c.1196T>C | NP_001341551.1:p.Ile399Thr | |
| NM_001354623.1:c.1196T>C | NP_001341552.1:p.Ile399Thr | |
| NM_001354624.1:c.1145T>C | NP_001341553.1:p.Ile382Thr | |
| NM_001354625.1:c.1145T>C | NP_001341554.1:p.Ile382Thr | |
| NM_001354626.1:c.1145T>C | NP_001341555.1:p.Ile382Thr | |
| NM_001354627.1:c.1145T>C | NP_001341556.1:p.Ile382Thr | |
| NM_001354628.1:c.2126T>C | NP_001341557.1:p.Ile709Thr | |
| NM_001354629.1:c.2120T>C | NP_001341558.1:p.Ile707Thr | |
| NM_001354630.1:c.2054T>C | NP_001341559.1:p.Ile685Thr | |
| XM_005265161.2:c.2012T>C | XP_005265218.1:p.Ile671Thr | |
| XM_017006450.2:c.1196T>C | XP_016861939.1:p.Ile399Thr | |
| NM_000249.4:c.2219T>C MANE Select | NP_000240.1:p.Ile740Thr | |
| NM_001167617.3:c.1925T>C | NP_001161089.1:p.Ile642Thr | |
| NM_001167618.3:c.1496T>C | NP_001161090.1:p.Ile499Thr | |
| NM_001167619.3:c.1496T>C | NP_001161091.1:p.Ile499Thr | |
| NM_001258271.2:c.2012T>C | NP_001245200.1:p.Ile671Thr | |
| NM_001258273.2:c.1496T>C | NP_001245202.1:p.Ile499Thr | |
| NM_001258274.3:c.1496T>C | NP_001245203.1:p.Ile499Thr | |
| NM_001354615.2:c.1496T>C | NP_001341544.1:p.Ile499Thr | |
| NM_001354616.2:c.1496T>C | NP_001341545.1:p.Ile499Thr | |
| NM_001354617.2:c.1496T>C | NP_001341546.1:p.Ile499Thr | |
| NM_001354618.2:c.1496T>C | NP_001341547.1:p.Ile499Thr | |
| NM_001354619.2:c.1496T>C | NP_001341548.1:p.Ile499Thr | |
| NM_001354620.2:c.1925T>C | NP_001341549.1:p.Ile642Thr | |
| NM_001354621.2:c.1196T>C | NP_001341550.1:p.Ile399Thr | |
| NM_001354622.2:c.1196T>C | NP_001341551.1:p.Ile399Thr | |
| NM_001354623.2:c.1196T>C | NP_001341552.1:p.Ile399Thr | |
| NM_001354624.2:c.1145T>C | NP_001341553.1:p.Ile382Thr | |
| NM_001354625.2:c.1145T>C | NP_001341554.1:p.Ile382Thr | |
| NM_001354626.2:c.1145T>C | NP_001341555.1:p.Ile382Thr | |
| NM_001354627.2:c.1145T>C | NP_001341556.1:p.Ile382Thr | |
| NM_001354628.2:c.2126T>C | NP_001341557.1:p.Ile709Thr | |
| NM_001354629.2:c.2120T>C | NP_001341558.1:p.Ile707Thr | |
| NM_001354630.2:c.2054T>C | NP_001341559.1:p.Ile685Thr |