Linked Data
dbSNP Id:
rs370793686
ExAC:
11:66283086 C / A
gnomAD v2:
11-66283086-C-A
gnomAD v3:
11-66515615-C-A
gnomAD v4:
11-66515615-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.66515615C>A , CM000673.2:g.66515615C>A | GRCh38 |
| NC_000011.9:g.66283086C>A , CM000673.1:g.66283086C>A | GRCh37 |
| NC_000011.8:g.66039662C>A | NCBI36 |
| NG_009093.1:g.9968C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318312.12:c.479+29C>A MANE Select | ENSP00000317469.7:n.479+29C>A | |
| ENST00000318312.11:c.479+29C>A | ENSP00000317469.7:n.479+29C>A | |
| ENST00000393994.4:c.479+29C>A | ENSP00000377563.2:n.479+29C>A | |
| ENST00000419755.3:c.590+29C>A | ENSP00000398526.3:n.590+29C>A | |
| ENST00000455748.6:c.432+937C>A | ENSP00000405764.2:n.432+937C>A | |
| ENST00000524458.5:c.*140-78C>A | ENSP00000436195.1:n.*140-78C>A | |
| ENST00000524907.5:n.498C>A | ||
| ENST00000525809.5:c.206+29C>A | ENSP00000431187.1:n.206+29C>A | |
| ENST00000526035.5:c.*186+29C>A | ENSP00000434197.1:n.*186+29C>A | |
| ENST00000526760.5:c.*186+29C>A | ENSP00000432140.1:n.*186+29C>A | |
| ENST00000527251.5:c.*186+29C>A | ENSP00000434360.1:n.*186+29C>A | |
| ENST00000529766.5:n.486+29C>A | ||
| ENST00000529953.5:n.131+29C>A | ||
| ENST00000529955.5:n.451-78C>A | ||
| ENST00000532908.5:c.*140-78C>A | ENSP00000431866.1:n.*140-78C>A | |
| ENST00000533430.5:n.257+29C>A | ||
| ENST00000533557.5:c.*140-78C>A | ENSP00000434619.1:n.*140-78C>A | |
| ENST00000533644.5:c.433-78C>A | ENSP00000436073.1:n.433-78C>A | |
| ENST00000534730.5:n.491+29C>A | ||
| ENST00000630659.2:c.*186+29C>A | ENSP00000486455.1:n.*186+29C>A | |
| NM_024649.4:c.479+29C>A | NP_078925.3:n.479+29C>A | |
| NM_024649.5:c.479+29C>A MANE Select | NP_078925.3:n.479+29C>A |