Linked Data
ClinVar Variation Id:
486852
dbSNP Id:
rs780141938
ExAC:
3:37038197 C / G
gnomAD v2:
3-37038197-C-G
gnomAD v4:
3-36996706-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.36996706C>G , CM000665.2:g.36996706C>G | GRCh38 |
| NC_000003.11:g.37038197C>G , CM000665.1:g.37038197C>G | GRCh37 |
| NC_000003.10:g.37013201C>G | NCBI36 |
| NG_007109.2:g.8357C>G , LRG_216:g.8357C>G | |
| NG_008418.1:g.1599G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000413740.2:c.204C>G | ENSP00000416476.2:p.Ile68Met | |
| ENST00000429117.6:c.-86C>G | ENSP00000407019.2:n.-86C>G | |
| ENST00000450420.6:c.204C>G | ENSP00000393006.2:p.Ile68Met | |
| ENST00000456676.7:c.204C>G | ENSP00000416687.3:p.Ile68Met | |
| ENST00000458009.6:c.204C>G | ENSP00000411066.2:p.Ile68Met | |
| ENST00000492474.6:c.-520C>G | ENSP00000518393.1:n.-520C>G | |
| ENST00000616768.6:c.204C>G | ENSP00000480669.3:p.Ile68Met | |
| ENST00000673673.2:c.204C>G | ENSP00000500979.2:p.Ile68Met | |
| ENST00000231790.8:c.204C>G MANE Select | ENSP00000231790.3:p.Ile68Met | |
| ENST00000413212.2:c.-520C>G | ENSP00000400844.2:n.-520C>G | |
| ENST00000432299.6:c.*284C>G | ENSP00000416783.1:n.*284C>G | |
| ENST00000441265.6:c.-520C>G | ENSP00000398392.2:n.-520C>G | |
| ENST00000442249.6:n.219C>G | ||
| ENST00000447829.6:c.-86C>G | ENSP00000399329.2:n.-86C>G | |
| ENST00000476172.6:n.1120-1264C>G | ||
| ENST00000539477.6:c.-428C>G | ENSP00000443665.1:n.-428C>G | |
| ENST00000673673.1:c.157C>G | ||
| ENST00000673686.1:n.194C>G | ||
| ENST00000673713.1:n.235C>G | ||
| ENST00000673715.1:c.204C>G | ENSP00000501301.1:p.Ile68Met | |
| ENST00000673897.1:c.116+3043C>G | ENSP00000501109.1:n.116+3043C>G | |
| ENST00000673899.1:c.204C>G | ENSP00000501030.1:p.Ile68Met | |
| ENST00000673947.1:c.*344C>G | ENSP00000501304.1:n.*344C>G | |
| ENST00000673972.1:c.*82C>G | ENSP00000501281.1:n.*82C>G | |
| ENST00000673990.1:n.189C>G | ||
| ENST00000674019.1:c.-520C>G | ENSP00000501081.1:n.-520C>G | |
| ENST00000674107.1:n.146C>G | ||
| ENST00000674111.1:c.204C>G | ENSP00000501162.1:p.Ile68Met | |
| ENST00000231790.6:c.204C>G | ENSP00000231790.2:p.Ile68Met | |
| ENST00000429117.5:c.-86C>G | ENSP00000407019.1:n.-86C>G | |
| ENST00000432299.5:c.*284C>G | ENSP00000416783.1:n.*284C>G | |
| ENST00000435176.5:c.-86C>G | ENSP00000402564.1:n.-86C>G | |
| ENST00000441265.5:c.-428C>G | ENSP00000398392.1:n.-428C>G | |
| ENST00000442249.5:c.116+3043C>G | ENSP00000387511.1:n.116+3043C>G | |
| ENST00000454028.5:c.*82C>G | ENSP00000392649.1:n.*82C>G | |
| ENST00000455445.6:c.-520C>G | ENSP00000398272.2:n.-520C>G | |
| ENST00000456676.6:c.179C>G | ||
| ENST00000457004.5:c.*82C>G | ENSP00000407773.1:n.*82C>G | |
| ENST00000458205.6:c.-665C>G | ENSP00000402667.2:n.-665C>G | |
| ENST00000466900.5:n.131C>G | ||
| ENST00000476172.5:n.326C>G | ||
| ENST00000485889.1:n.208C>G | ||
| ENST00000492474.5:n.227C>G | ||
| ENST00000536378.5:c.-517+3043C>G | ENSP00000444286.2:n.-517+3043C>G | |
| ENST00000539477.5:c.-428C>G | ENSP00000443665.1:n.-428C>G | |
| NM_000249.3:c.204C>G , LRG_216t1:c.204C>G | NP_000240.1:p.Ile68Met | |
| NM_001167617.1:c.-86C>G | NP_001161089.1:n.-86C>G | |
| NM_001167618.1:c.-520C>G | NP_001161090.1:n.-520C>G | |
| NM_001167619.1:c.-428C>G | NP_001161091.1:n.-428C>G | |
| NM_001258271.1:c.204C>G | NP_001245200.1:p.Ile68Met | |
| NM_001258273.1:c.-517+3043C>G | NP_001245202.1:n.-517+3043C>G | |
| NM_001258274.1:c.-665C>G | NP_001245203.1:n.-665C>G | |
| XM_005265161.1:c.204C>G | XP_005265218.1:p.Ile68Met | |
| XM_005265163.1:c.-520C>G | XP_005265220.1:n.-520C>G | |
| XM_005265164.1:c.-520C>G | XP_005265221.1:n.-520C>G | |
| XM_005265166.1:c.-726C>G | XP_005265223.1:n.-726C>G | |
| XM_011533727.1:c.-623C>G | XP_011532029.1:n.-623C>G | |
| NM_001167617.2:c.-86C>G | NP_001161089.1:n.-86C>G | |
| NM_001167618.2:c.-520C>G | NP_001161090.1:n.-520C>G | |
| NM_001167619.2:c.-428C>G | NP_001161091.1:n.-428C>G | |
| NM_001258274.2:c.-665C>G | NP_001245203.1:n.-665C>G | |
| NM_001354615.1:c.-423C>G | NP_001341544.1:n.-423C>G | |
| NM_001354616.1:c.-428C>G | NP_001341545.1:n.-428C>G | |
| NM_001354617.1:c.-520C>G | NP_001341546.1:n.-520C>G | |
| NM_001354618.1:c.-520C>G | NP_001341547.1:n.-520C>G | |
| NM_001354619.1:c.-520C>G | NP_001341548.1:n.-520C>G | |
| NM_001354620.1:c.-86C>G | NP_001341549.1:n.-86C>G | |
| NM_001354621.1:c.-613C>G | NP_001341550.1:n.-613C>G | |
| NM_001354622.1:c.-726C>G | NP_001341551.1:n.-726C>G | |
| NM_001354623.1:c.-723+2816C>G | NP_001341552.1:n.-723+2816C>G | |
| NM_001354624.1:c.-623C>G | NP_001341553.1:n.-623C>G | |
| NM_001354625.1:c.-526C>G | NP_001341554.1:n.-526C>G | |
| NM_001354626.1:c.-623C>G | NP_001341555.1:n.-623C>G | |
| NM_001354627.1:c.-623C>G | NP_001341556.1:n.-623C>G | |
| NM_001354628.1:c.204C>G | NP_001341557.1:p.Ile68Met | |
| NM_001354629.1:c.204C>G | NP_001341558.1:p.Ile68Met | |
| NM_001354630.1:c.204C>G | NP_001341559.1:p.Ile68Met | |
| XM_005265161.2:c.204C>G | XP_005265218.1:p.Ile68Met | |
| XM_017006450.2:c.-613C>G | XP_016861939.1:n.-613C>G | |
| NM_000249.4:c.204C>G MANE Select | NP_000240.1:p.Ile68Met | |
| NM_001167617.3:c.-86C>G | NP_001161089.1:n.-86C>G | |
| NM_001167618.3:c.-520C>G | NP_001161090.1:n.-520C>G | |
| NM_001167619.3:c.-428C>G | NP_001161091.1:n.-428C>G | |
| NM_001258271.2:c.204C>G | NP_001245200.1:p.Ile68Met | |
| NM_001258273.2:c.-517+3043C>G | NP_001245202.1:n.-517+3043C>G | |
| NM_001258274.3:c.-665C>G | NP_001245203.1:n.-665C>G | |
| NM_001354615.2:c.-423C>G | NP_001341544.1:n.-423C>G | |
| NM_001354616.2:c.-428C>G | NP_001341545.1:n.-428C>G | |
| NM_001354617.2:c.-520C>G | NP_001341546.1:n.-520C>G | |
| NM_001354618.2:c.-520C>G | NP_001341547.1:n.-520C>G | |
| NM_001354619.2:c.-520C>G | NP_001341548.1:n.-520C>G | |
| NM_001354620.2:c.-86C>G | NP_001341549.1:n.-86C>G | |
| NM_001354621.2:c.-613C>G | NP_001341550.1:n.-613C>G | |
| NM_001354622.2:c.-726C>G | NP_001341551.1:n.-726C>G | |
| NM_001354623.2:c.-723+2816C>G | NP_001341552.1:n.-723+2816C>G | |
| NM_001354624.2:c.-623C>G | NP_001341553.1:n.-623C>G | |
| NM_001354625.2:c.-526C>G | NP_001341554.1:n.-526C>G | |
| NM_001354626.2:c.-623C>G | NP_001341555.1:n.-623C>G | |
| NM_001354627.2:c.-623C>G | NP_001341556.1:n.-623C>G | |
| NM_001354628.2:c.204C>G | NP_001341557.1:p.Ile68Met | |
| NM_001354629.2:c.204C>G | NP_001341558.1:p.Ile68Met | |
| NM_001354630.2:c.204C>G | NP_001341559.1:p.Ile68Met |