Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22625484G= , CM000673.2:g.22625484G= | GRCh38 |
| NC_000011.9:g.22647030G= , CM000673.1:g.22647030G= | GRCh37 |
| NC_000011.8:g.22603606G= | NCBI36 |
| NG_007425.1:g.5358C= , LRG_527:g.5358C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022725.4:c.327C= MANE Select | NP_073562.1:p.Tyr109= |
| ENST00000327470.6:c.327C= MANE Select | ENSP00000330875.3:p.Tyr109= |
| NM_022725.3:c.327C= , LRG_527t1:c.327C= | NP_073562.1:p.Tyr109= |
| ENST00000327470.4:c.327C= | ENSP00000330875.3:p.Tyr109= |