Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22625386G= , CM000673.2:g.22625386G= | GRCh38 |
| NC_000011.9:g.22646932G= , CM000673.1:g.22646932G= | GRCh37 |
| NC_000011.8:g.22603508G= | NCBI36 |
| NG_007425.1:g.5456C= , LRG_527:g.5456C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327470.6:c.425C= MANE Select | ENSP00000330875.3:p.Ala142= | |
| ENST00000327470.4:c.425C= | ENSP00000330875.3:p.Ala142= | |
| NM_022725.3:c.425C= , LRG_527t1:c.425C= | NP_073562.1:p.Ala142= | |
| NM_022725.4:c.425C= MANE Select | NP_073562.1:p.Ala142= |