Linked Data
dbSNP Id:
rs1562343302
gnomAD v2:
6-157520029-C-T
gnomAD v3:
6-157198895-C-T
gnomAD v4:
6-157198895-C-T
MyVariant Identifiers:
chr6:g.157520029C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.157198895C>T , CM000668.2:g.157198895C>T | GRCh38 |
| NC_000006.11:g.157520029C>T , CM000668.1:g.157520029C>T | GRCh37 |
| NC_000006.10:g.157561721C>T | NCBI36 |
| NG_032093.1:g.425966C>T | |
| NG_032093.2:g.425966C>T | |
| NG_066624.1:g.427870C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000350026.11:c.4308C>T | ENSP00000055163.8:p.Tyr1436= | |
| ENST00000414678.8:c.4377C>T | ENSP00000412835.3:p.Tyr1459= | |
| ENST00000637015.2:c.4596C>T | ENSP00000489729.2:p.Tyr1532= | |
| ENST00000346085.10:c.4347C>T | ENSP00000344546.5:p.Tyr1449= | |
| ENST00000350026.10:c.4059C>T | ENSP00000055163.7:p.Tyr1353= | |
| ENST00000414678.7:c.2625C>T | ENSP00000412835.2:p.Tyr875= | |
| ENST00000635849.1:c.1788C>T | ENSP00000490948.1:p.Tyr596= | |
| ENST00000635957.1:c.1419C>T | ENSP00000490385.1:p.Tyr473= | |
| ENST00000636227.1:n.2930C>T | ||
| ENST00000636254.1:n.387C>T | ||
| ENST00000636930.2:c.4467C>T MANE Select | ENSP00000490491.2:p.Tyr1489= | |
| ENST00000636940.1:n.2464C>T | ||
| ENST00000637015.1:c.1835C>T | ||
| ENST00000637568.1:c.1749C>T | ||
| ENST00000637741.1:n.1133C>T | ||
| ENST00000637810.1:c.1809C>T | ENSP00000489636.1:p.Tyr603= | |
| ENST00000637904.1:c.1968C>T | ENSP00000490550.1:p.Tyr656= | |
| ENST00000647938.1:c.4098C>T | ENSP00000498155.1:p.Tyr1366= | |
| ENST00000346085.9:c.4098C>T | ENSP00000344546.4:p.Tyr1366= | |
| ENST00000350026.9:c.4059C>T | ENSP00000055163.7:p.Tyr1353= | |
| ENST00000414678.6:c.2625C>T | ENSP00000412835.2:p.Tyr875= | |
| NM_017519.2:c.4059C>T | NP_059989.2:p.Tyr1353= | |
| NM_020732.3:c.4098C>T | NP_065783.3:p.Tyr1366= | |
| XM_005267069.3:c.4218C>T | XP_005267126.2:p.Tyr1406= | |
| XM_011535984.1:c.3297C>T | XP_011534286.1:p.Tyr1099= | |
| XM_011535985.1:c.3117C>T | XP_011534287.1:p.Tyr1039= | |
| XM_011535986.1:c.2877C>T | XP_011534288.1:p.Tyr959= | |
| XM_011535987.1:c.2496C>T | XP_011534289.1:p.Tyr832= | |
| XM_011535988.1:c.1359C>T | XP_011534290.1:p.Tyr453= | |
| NM_001346813.1:c.4218C>T | NP_001333742.1:p.Tyr1406= | |
| NM_001363725.1:c.1968C>T | NP_001350654.1:p.Tyr656= | |
| XM_011535984.2:c.4428C>T | XP_011534286.2:p.Tyr1476= | |
| XM_011535988.3:c.1359C>T | XP_011534290.1:p.Tyr453= | |
| XM_017011103.2:c.4329C>T | XP_016866592.1:p.Tyr1443= | |
| XM_017011104.1:c.4299C>T | XP_016866593.1:p.Tyr1433= | |
| XM_017011105.2:c.4269C>T | XP_016866594.1:p.Tyr1423= | |
| XM_017011106.2:c.4140C>T | XP_016866595.1:p.Tyr1380= | |
| XM_017011107.2:c.4119C>T | XP_016866596.1:p.Tyr1373= | |
| XR_002956289.1:n.4427-1810C>T | ||
| NM_001363725.2:c.1968C>T | NP_001350654.1:p.Tyr656= | |
| NM_001371656.1:c.4347C>T | NP_001358585.1:p.Tyr1449= | |
| NM_001374820.1:c.4347C>T | NP_001361749.1:p.Tyr1449= | |
| NM_001374828.1:c.4467C>T MANE Select | NP_001361757.1:p.Tyr1489= | |
| NM_017519.3:c.4308C>T | NP_059989.3:p.Tyr1436= |