Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48633435T= , CM000681.2:g.48633435T= | GRCh38 |
| NC_000019.9:g.49136692T= , CM000681.1:g.49136692T= | GRCh37 |
| NC_000019.8:g.53828504T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222122.10:c.762+9A= MANE Select | ENSP00000222122.4:n.762+9A= | |
| ENST00000222122.9:c.762+9A= | ENSP00000222122.4:n.762+9A= | |
| ENST00000593500.1:c.156+9A= | ENSP00000471220.1:n.156+9A= | |
| ENST00000594723.1:n.3014A= | ||
| ENST00000599385.5:c.156+9A= | ENSP00000469426.1:n.156+9A= | |
| ENST00000601104.1:c.771A= | ENSP00000469291.1:p.Arg257= | |
| NM_001352.4:c.762+9A= | NP_001343.2:n.762+9A= | |
| XM_017026388.2:c.333+9A= | XP_016881877.1:n.333+9A= | |
| XR_243907.4:n.1667+9A= | ||
| NM_001352.5:c.762+9A= MANE Select | NP_001343.2:n.762+9A= |