Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.80591716G= , CM000677.2:g.80591716G= | GRCh38 |
| NC_000015.9:g.80884057G= , CM000677.1:g.80884057G= | GRCh37 |
| NC_000015.8:g.78671112G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303329.9:c.2055+12G= MANE Select | ENSP00000307479.4:n.2055+12G= | |
| ENST00000303329.8:c.2055+12G= | ENSP00000307479.4:n.2055+12G= | |
| ENST00000527771.5:c.2022+12G= | ENSP00000453792.1:n.2022+12G= | |
| ENST00000533983.5:c.2022+12G= | ENSP00000453651.1:n.2022+12G= | |
| ENST00000610490.4:c.*353+12G= | ENSP00000483762.1:n.*353+12G= | |
| ENST00000622346.4:c.2055+12G= | ENSP00000479393.1:n.2055+12G= | |
| NM_014862.3:c.2055+12G= | NP_055677.3:n.2055+12G= | |
| NM_014862.4:c.2055+12G= MANE Select | NP_055677.3:n.2055+12G= |