Linked Data
ClinVar Variation Id:
330915
dbSNP Id:
rs200898383
ExAC:
2:11923983 C / T
gnomAD v2:
2-11923983-C-T
gnomAD v3:
2-11783857-C-T
gnomAD v4:
2-11783857-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.11783857C>T , CM000664.2:g.11783857C>T | GRCh38 |
| NC_000002.11:g.11923983C>T , CM000664.1:g.11923983C>T | GRCh37 |
| NC_000002.10:g.11841434C>T | NCBI36 |
| NG_012843.2:g.111279C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000674199.1:c.1293C>T MANE Select | ENSP00000501331.1:p.Asp431= | |
| ENST00000256720.6:c.1185C>T | ENSP00000256720.2:p.Asp395= | |
| ENST00000396097.5:c.1311C>T | ENSP00000379404.2:p.Asp437= | |
| ENST00000396098.5:c.1311C>T | ENSP00000379405.1:p.Asp437= | |
| ENST00000396099.5:c.1311C>T | ENSP00000379406.2:p.Asp437= | |
| ENST00000404113.6:n.778C>T | ||
| ENST00000425416.6:c.1203C>T | ENSP00000401522.2:p.Asp401= | |
| ENST00000449576.6:c.1440C>T | ENSP00000397908.2:p.Asp480= | |
| ENST00000460096.1:n.173C>T | ||
| NM_001261427.1:c.1203C>T | NP_001248356.1:p.Asp401= | |
| NM_001261428.1:c.1440C>T | NP_001248357.1:p.Asp480= | |
| NM_001261429.1:c.1311C>T | NP_001248358.1:p.Asp437= | |
| NM_145693.2:c.1185C>T | NP_663731.1:p.Asp395= | |
| XM_006711869.1:c.1332C>T | XP_006711932.1:p.Asp444= | |
| XM_006711870.2:c.1311C>T | XP_006711933.1:p.Asp437= | |
| XM_006711871.1:c.1293C>T | XP_006711934.1:p.Asp431= | |
| XM_006711872.1:c.1293C>T | XP_006711935.1:p.Asp431= | |
| XM_006711874.1:c.1293C>T | XP_006711937.1:p.Asp431= | |
| XM_011510333.1:c.1437C>T | XP_011508635.1:p.Asp479= | |
| XM_011510334.1:c.1311C>T | XP_011508636.1:p.Asp437= | |
| XM_011510335.1:c.1293C>T | XP_011508637.1:p.Asp431= | |
| XM_011510336.1:c.1293C>T | XP_011508638.1:p.Asp431= | |
| XM_011510337.1:c.1440C>T | XP_011508639.1:p.Asp480= | |
| XM_011510338.1:c.1440C>T | XP_011508640.1:p.Asp480= | |
| NM_001261427.2:c.1203C>T | NP_001248356.1:p.Asp401= | |
| NM_001261428.2:c.1440C>T | NP_001248357.1:p.Asp480= | |
| NM_001349199.1:c.1185C>T | NP_001336128.1:p.Asp395= | |
| NM_001349200.1:c.1185C>T | NP_001336129.1:p.Asp395= | |
| NM_001349201.1:c.1185C>T | NP_001336130.1:p.Asp395= | |
| NM_001349202.1:c.1290C>T | NP_001336131.1:p.Asp430= | |
| NM_001349203.1:c.1290C>T | NP_001336132.1:p.Asp430= | |
| NM_001349204.1:c.1293C>T | NP_001336133.1:p.Asp431= | |
| NM_001349205.1:c.1293C>T | NP_001336134.1:p.Asp431= | |
| NM_001349206.1:c.1293C>T | NP_001336135.1:p.Asp431= | |
| NM_001349207.1:c.1383C>T | NP_001336136.1:p.Asp461= | |
| NM_001349208.1:c.1332C>T | NP_001336137.1:p.Asp444= | |
| NM_145693.3:c.1185C>T | NP_663731.1:p.Asp395= | |
| NR_146080.1:n.1281C>T | ||
| XM_006711870.4:c.1311C>T | XP_006711933.1:p.Asp437= | |
| XM_006711872.3:c.1293C>T | XP_006711935.1:p.Asp431= | |
| XM_011510333.2:c.1437C>T | XP_011508635.1:p.Asp479= | |
| XM_011510334.3:c.1311C>T | XP_011508636.1:p.Asp437= | |
| XM_011510335.3:c.1293C>T | XP_011508637.1:p.Asp431= | |
| XM_011510336.3:c.1293C>T | XP_011508638.1:p.Asp431= | |
| XM_017003623.2:c.1362C>T | XP_016859112.1:p.Asp454= | |
| XM_017003624.2:c.1293C>T | XP_016859113.1:p.Asp431= | |
| XM_017003625.2:c.1293C>T | XP_016859114.1:p.Asp431= | |
| XM_017003627.2:c.1290C>T | XP_016859116.1:p.Asp430= | |
| XM_017003628.2:c.1185C>T | XP_016859117.1:p.Asp395= | |
| XM_017003629.1:c.1185C>T | XP_016859118.1:p.Asp395= | |
| XM_017003630.2:c.1185C>T | XP_016859119.1:p.Asp395= | |
| XM_017003631.1:c.1293C>T | XP_016859120.1:p.Asp431= | |
| XM_024452762.1:c.1293C>T | XP_024308530.1:p.Asp431= | |
| XM_024452763.1:c.1203C>T | XP_024308531.1:p.Asp401= | |
| NM_001261428.3:c.1440C>T | NP_001248357.1:p.Asp480= | |
| NM_001349199.2:c.1185C>T | NP_001336128.1:p.Asp395= | |
| NM_001349200.2:c.1185C>T | NP_001336129.1:p.Asp395= | |
| NM_001349201.2:c.1185C>T | NP_001336130.1:p.Asp395= | |
| NM_001349202.2:c.1290C>T | NP_001336131.1:p.Asp430= | |
| NM_001349203.2:c.1290C>T | NP_001336132.1:p.Asp430= | |
| NM_001349204.2:c.1293C>T | NP_001336133.1:p.Asp431= | |
| NM_001349206.2:c.1293C>T MANE Select | NP_001336135.1:p.Asp431= | |
| NM_001349207.2:c.1383C>T | NP_001336136.1:p.Asp461= | |
| NM_001349208.2:c.1332C>T | NP_001336137.1:p.Asp444= | |
| NM_145693.4:c.1185C>T | NP_663731.1:p.Asp395= | |
| NR_146080.2:n.1234C>T | ||
| NM_001261427.3:c.1203C>T | NP_001248356.1:p.Asp401= | |
| NM_001349205.2:c.1293C>T | NP_001336134.1:p.Asp431= |