Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.22812252G= , CM000677.2:g.22812252G= | GRCh38 |
| NC_000015.9:g.23060816C= , CM000677.1:g.23060816C= | GRCh37 |
| NC_000015.8:g.20612257C= | NCBI36 |
| NG_009056.1:g.31028G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_144599.5:c.316G= MANE Select | NP_653200.2:p.Gly106= |
| ENST00000337435.9:c.316G= MANE Select | ENSP00000337452.4:p.Gly106= |
| NM_001142275.1:c.91G= | NP_001135747.1:p.Gly31= |
| NM_144599.4:c.316G= | NP_653200.2:p.Gly106= |
| ENST00000337435.8:c.316G= | ENSP00000337452.4:p.Gly106= |
| ENST00000437912.6:c.91G= | ENSP00000393962.2:p.Gly31= |
| ENST00000557930.1:c.160G= | ENSP00000453797.1:p.Gly54= |
| ENST00000559448.5:c.206G= | |
| ENST00000560069.5:n.169G= | |
| ENST00000561183.5:c.91G= | ENSP00000453722.1:p.Gly31= |