Linked Data
ClinVar Variation Id:
2772688
ClinVar RCV Id:
RCV003576799
dbSNP Id:
rs752776372
ExAC:
3:48610091 G / A
gnomAD v2:
3-48610091-G-A
gnomAD v4:
3-48572658-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.48572658G>A , CM000665.2:g.48572658G>A | GRCh38 |
| NC_000003.11:g.48610091G>A , CM000665.1:g.48610091G>A | GRCh37 |
| NC_000003.10:g.48585095G>A | NCBI36 |
| NG_007065.1:g.27595C>T , LRG_286:g.27595C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000681320.1:c.6900+13C>T MANE Select | ENSP00000506558.1:n.6900+13C>T | |
| ENST00000328333.12:c.6900+13C>T | ENSP00000332371.8:n.6900+13C>T | |
| ENST00000487017.5:n.2817+13C>T | ||
| NM_000094.3:c.6900+13C>T , LRG_286t1:c.6900+13C>T | NP_000085.1:n.6900+13C>T | |
| XM_011533336.1:c.6927+13C>T | XP_011531638.1:n.6927+13C>T | |
| XM_011533337.1:c.6900+13C>T | XP_011531639.1:n.6900+13C>T | |
| XM_011533338.1:c.6927+13C>T | XP_011531640.1:n.6927+13C>T | |
| XM_011533339.1:c.6927+13C>T | XP_011531641.1:n.6927+13C>T | |
| XM_011533340.1:c.6927+13C>T | XP_011531642.1:n.6927+13C>T | |
| XM_011533341.1:c.6927+13C>T | XP_011531643.1:n.6927+13C>T | |
| XM_011533342.1:c.6927+13C>T | XP_011531644.1:n.6927+13C>T | |
| XR_940369.1:n.6963+13C>T | ||
| XR_940370.1:n.6963+13C>T | ||
| XR_940371.1:n.6963+13C>T | ||
| XR_940372.1:n.6963+13C>T | ||
| XR_940373.1:n.6963+13C>T | ||
| XR_940374.1:n.6973+13C>T | ||
| XM_017005688.1:c.6900+13C>T | XP_016861177.1:n.6900+13C>T | |
| XM_017005689.1:c.6900+13C>T | XP_016861178.1:n.6900+13C>T | |
| XM_017005690.1:c.6900+13C>T | XP_016861179.1:n.6900+13C>T | |
| XM_017005691.1:c.6900+13C>T | XP_016861180.1:n.6900+13C>T | |
| XM_017005692.1:c.6900+13C>T | XP_016861181.1:n.6900+13C>T | |
| XR_001740003.1:n.6936+13C>T | ||
| XR_001740004.1:n.6936+13C>T | ||
| XR_001740005.1:n.6936+13C>T | ||
| XR_001740006.1:n.6936+13C>T | ||
| XR_001740007.1:n.6936+13C>T | ||
| XR_001740008.1:n.6946+13C>T | ||
| NM_000094.4:c.6900+13C>T MANE Select | NP_000085.1:n.6900+13C>T |