Linked Data
ClinVar Variation Id:
366542
dbSNP Id:
rs116483820
ExAC:
9:304717 A / G
gnomAD v2:
9-304717-A-G
gnomAD v3:
9-304717-A-G
gnomAD v4:
9-304717-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.304717A>G , CM000671.2:g.304717A>G | GRCh38 |
| NC_000009.11:g.304717A>G , CM000671.1:g.304717A>G | GRCh37 |
| NC_000009.10:g.294717A>G | NCBI36 |
| NG_017007.1:g.94853A>G , LRG_196:g.94853A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382329.2:c.324+13A>G | ENSP00000371766.2:n.324+13A>G | |
| ENST00000483757.6:c.324+13A>G | ENSP00000417691.2:n.324+13A>G | |
| ENST00000682249.1:c.324+13A>G | ENSP00000507731.1:n.324+13A>G | |
| ENST00000684384.1:n.637+13A>G | ||
| ENST00000432829.7:c.528+13A>G MANE Select | ENSP00000394888.3:n.528+13A>G | |
| ENST00000382341.5:n.423+13A>G | ||
| ENST00000432829.6:c.528+13A>G | ENSP00000394888.3:n.528+13A>G | |
| ENST00000453981.5:c.324+13A>G | ENSP00000408464.2:n.324+13A>G | |
| ENST00000454469.6:n.637+13A>G | ||
| ENST00000469391.5:c.324+13A>G | ENSP00000419438.1:n.324+13A>G | |
| ENST00000478380.5:n.407+13A>G | ||
| ENST00000483757.5:c.324+13A>G | ENSP00000417691.1:n.324+13A>G | |
| ENST00000495184.5:n.389+13A>G | ||
| ENST00000524396.5:c.*491+13A>G | ENSP00000436628.1:n.*491+13A>G | |
| NM_001190458.1:c.324+13A>G | NP_001177387.1:n.324+13A>G | |
| NM_001193536.1:c.324+13A>G | NP_001180465.1:n.324+13A>G | |
| NM_203447.3:c.528+13A>G , LRG_196t1:c.528+13A>G | NP_982272.2:n.528+13A>G | |
| XM_011518045.1:c.324+13A>G | XP_011516347.1:n.324+13A>G | |
| XM_011518046.1:c.390+13A>G | XP_011516348.1:n.390+13A>G | |
| XM_011518047.1:c.324+13A>G | XP_011516349.1:n.324+13A>G | |
| XM_011518048.1:c.324+13A>G | XP_011516350.1:n.324+13A>G | |
| XM_011518045.3:c.324+13A>G | XP_011516347.1:n.324+13A>G | |
| XM_011518046.2:c.390+13A>G | XP_011516348.1:n.390+13A>G | |
| XM_011518047.3:c.324+13A>G | XP_011516349.1:n.324+13A>G | |
| XM_011518048.2:c.324+13A>G | XP_011516350.1:n.324+13A>G | |
| XM_017015173.1:c.324+13A>G | XP_016870662.1:n.324+13A>G | |
| XM_017015174.1:c.390+13A>G | XP_016870663.1:n.390+13A>G | |
| NM_001190458.2:c.324+13A>G | NP_001177387.1:n.324+13A>G | |
| NM_001193536.2:c.324+13A>G | NP_001180465.1:n.324+13A>G | |
| NM_203447.4:c.528+13A>G MANE Select | NP_982272.2:n.528+13A>G |