Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48527059T= , CM000685.2:g.48527059T= | GRCh38 |
| NC_000023.10:g.48385447T= , CM000685.1:g.48385447T= | GRCh37 |
| NC_000023.9:g.48270391T= | NCBI36 |
| NG_007452.1:g.10284T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000495186.6:c.338+34T= MANE Select | ENSP00000417052.1:n.338+34T= | |
| ENST00000651615.1:c.338+34T= | ENSP00000498524.1:n.338+34T= | |
| ENST00000276096.10:n.296+34T= | ||
| ENST00000414061.1:c.338+34T= | ENSP00000405832.1:n.338+34T= | |
| ENST00000446158.5:c.338+34T= | ENSP00000390031.1:n.338+34T= | |
| ENST00000466461.1:n.177+34T= | ||
| ENST00000495186.5:c.338+34T= | ENSP00000417052.1:n.338+34T= | |
| ENST00000498425.1:n.459+34T= | ||
| NM_006579.2:c.338+34T= | NP_006570.1:n.338+34T= | |
| NM_006579.3:c.338+34T= MANE Select | NP_006570.1:n.338+34T= |