Linked Data
dbSNP Id:
rs551605985
gnomAD v2:
5-68729065-C-T
gnomAD v3:
5-69433238-C-T
gnomAD v4:
5-69433238-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.69433238C>T , CM000667.2:g.69433238C>T | GRCh38 |
| NC_000005.9:g.68729065C>T , CM000667.1:g.68729065C>T | GRCh37 |
| NC_000005.8:g.68764821C>T | NCBI36 |
| NG_017201.1:g.23127C>T | |
| NG_017201.2:g.23127C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325631.10:c.1503+145C>T MANE Select | ENSP00000323264.5:n.1503+145C>T | |
| ENST00000413223.3:c.1155+145C>T | ENSP00000398922.2:n.1155+145C>T | |
| ENST00000436532.7:c.1155+145C>T | ENSP00000414776.2:n.1155+145C>T | |
| ENST00000645446.1:c.1503+145C>T | ENSP00000494616.1:n.1503+145C>T | |
| ENST00000647531.1:c.1467+145C>T | ENSP00000493858.1:n.1467+145C>T | |
| ENST00000325631.9:c.1503+145C>T | ENSP00000323264.5:n.1503+145C>T | |
| ENST00000413223.2:c.1155+145C>T | ENSP00000398922.2:n.1155+145C>T | |
| ENST00000436532.6:c.1155+145C>T | ENSP00000414776.2:n.1155+145C>T | |
| ENST00000454295.6:c.1467+145C>T | ENSP00000396244.2:n.1467+145C>T | |
| ENST00000512803.5:c.1503+145C>T | ENSP00000423490.1:n.1503+145C>T | |
| NM_001038603.2:c.1503+145C>T | NP_001033692.2:n.1503+145C>T | |
| NM_001244734.1:c.1467+145C>T | NP_001231663.1:n.1467+145C>T | |
| XM_005248445.3:c.1503+145C>T | XP_005248502.1:n.1503+145C>T | |
| XM_005248446.3:c.1503+145C>T | XP_005248503.1:n.1503+145C>T | |
| XM_005248447.3:c.1467+145C>T | XP_005248504.1:n.1467+145C>T | |
| XM_005248445.4:c.1503+145C>T | XP_005248502.1:n.1503+145C>T | |
| XM_005248446.4:c.1503+145C>T | XP_005248503.1:n.1503+145C>T | |
| XM_005248447.4:c.1467+145C>T | XP_005248504.1:n.1467+145C>T | |
| NM_001038603.3:c.1503+145C>T MANE Select | NP_001033692.2:n.1503+145C>T | |
| NM_001244734.2:c.1467+145C>T | NP_001231663.1:n.1467+145C>T |