Linked Data
dbSNP Id:
rs369137031
gnomAD v4:
4-1806092-C-G
MyVariant Identifiers:
chr4:g.1807819C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.1806092C>G , CM000666.2:g.1806092C>G | GRCh38 |
| NC_000004.11:g.1807819C>G , CM000666.1:g.1807819C>G | GRCh37 |
| NC_000004.10:g.1777617C>G | NCBI36 |
| NG_012632.1:g.17781C>G , LRG_1021:g.17781C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340107.9:c.1884C>G | ENSP00000339824.4:p.Thr628= | |
| ENST00000260795.8:c.*934C>G | ENSP00000260795.3:n.*934C>G | |
| ENST00000352904.6:c.1542C>G | ENSP00000231803.1:p.Thr514= | |
| ENST00000412135.7:c.1866C>G | ENSP00000412903.3:p.Thr622= | |
| ENST00000440486.8:c.1878C>G MANE Select | ENSP00000414914.2:p.Thr626= | |
| ENST00000481110.7:c.1881C>G | ENSP00000420533.2:p.Thr627= | |
| ENST00000260795.6:c.1878C>G | ENSP00000260795.2:p.Thr626= | |
| ENST00000340107.8:c.1884C>G | ENSP00000339824.4:p.Thr628= | |
| ENST00000352904.5:c.1542C>G | ENSP00000231803.1:p.Thr514= | |
| ENST00000412135.6:c.1542C>G | ENSP00000412903.2:p.Thr514= | |
| ENST00000440486.6:c.1878C>G | ENSP00000414914.2:p.Thr626= | |
| ENST00000481110.6:c.1881C>G | ENSP00000420533.2:p.Thr627= | |
| ENST00000613647.4:c.*934C>G | ENSP00000479472.1:n.*934C>G | |
| NM_000142.4:c.1878C>G , LRG_1021t1:c.1878C>G | NP_000133.1:p.Thr626= | |
| NM_001163213.1:c.1884C>G , LRG_1021t2:c.1884C>G | NP_001156685.1:p.Thr628= | |
| NM_022965.3:c.1542C>G | NP_075254.1:p.Thr514= | |
| XM_006713868.1:c.1890C>G | XP_006713931.1:p.Thr630= | |
| XM_006713869.1:c.1890C>G | XP_006713932.1:p.Thr630= | |
| XM_006713870.1:c.1887C>G | XP_006713933.1:p.Thr629= | |
| XM_006713871.1:c.1884C>G | XP_006713934.1:p.Thr628= | |
| XM_006713872.1:c.1881C>G | XP_006713935.1:p.Thr627= | |
| XM_006713873.1:c.1878C>G | XP_006713936.1:p.Thr626= | |
| XM_011513420.1:c.1884C>G | XP_011511722.1:p.Thr628= | |
| XM_011513422.1:c.1881C>G | XP_011511724.1:p.Thr627= | |
| NM_001354809.1:c.1881C>G | NP_001341738.1:p.Thr627= | |
| NM_001354810.1:c.1881C>G | NP_001341739.1:p.Thr627= | |
| NR_148971.1:n.2285C>G | ||
| NM_001354809.2:c.1881C>G | NP_001341738.1:p.Thr627= | |
| NM_001354810.2:c.1881C>G | NP_001341739.1:p.Thr627= | |
| NR_148971.2:n.2304C>G | ||
| NM_000142.5:c.1878C>G MANE Select | NP_000133.1:p.Thr626= | |
| NM_001163213.2:c.1884C>G | NP_001156685.1:p.Thr628= | |
| NM_022965.4:c.1542C>G | NP_075254.1:p.Thr514= |