Linked Data
dbSNP Id:
rs4804134
ExAC:
19:10568519 T / A
gnomAD v2:
19-10568519-T-A
gnomAD v4:
19-10457843-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10457843T>A , CM000681.2:g.10457843T>A | GRCh38 |
| NC_000019.9:g.10568519T>A , CM000681.1:g.10568519T>A | GRCh37 |
| NC_000019.8:g.10429519T>A | NCBI36 |
| NG_029594.1:g.46071T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000380702.7:c.878-36T>A MANE Select | ENSP00000370078.3:n.878-36T>A | |
| ENST00000293683.9:c.800-36T>A | ENSP00000293683.4:n.800-36T>A | |
| ENST00000344979.7:c.161-36T>A | ENSP00000341007.2:n.161-36T>A | |
| ENST00000380702.6:c.878-36T>A | ENSP00000370078.3:n.878-36T>A | |
| ENST00000440014.6:c.695-36T>A | ENSP00000394754.1:n.695-36T>A | |
| ENST00000586275.1:n.141-36T>A | ||
| ENST00000589073.1:c.160+2921T>A | ENSP00000465792.1:n.160+2921T>A | |
| ENST00000591971.5:c.206-36T>A | ENSP00000467137.1:n.206-36T>A | |
| ENST00000592685.5:c.812-36T>A | ENSP00000468507.1:n.812-36T>A | |
| NM_001111307.1:c.878-36T>A | NP_001104777.1:n.878-36T>A | |
| NM_001111308.1:c.800-36T>A | NP_001104778.1:n.800-36T>A | |
| NM_001111309.1:c.695-36T>A | NP_001104779.1:n.695-36T>A | |
| NM_001243121.1:c.812-36T>A | NP_001230050.1:n.812-36T>A | |
| NM_006202.2:c.161-36T>A | NP_006193.1:n.161-36T>A | |
| XM_005259933.2:c.-35-36T>A | XP_005259990.1:n.-35-36T>A | |
| XM_011528054.1:c.812-36T>A | XP_011526356.1:n.812-36T>A | |
| XM_011528055.1:c.878-36T>A | XP_011526357.1:n.878-36T>A | |
| XM_011528055.3:c.878-36T>A | XP_011526357.1:n.878-36T>A | |
| XM_017026865.2:c.875-36T>A | XP_016882354.1:n.875-36T>A | |
| XM_024451534.1:c.-35-36T>A | XP_024307302.1:n.-35-36T>A | |
| NM_001111307.2:c.878-36T>A MANE Select | NP_001104777.1:n.878-36T>A | |
| NM_006202.3:c.161-36T>A | NP_006193.1:n.161-36T>A | |
| NM_001243121.2:c.812-36T>A | NP_001230050.1:n.812-36T>A |