Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23189600G= , CM000678.2:g.23189600G= | GRCh38 |
| NC_000016.9:g.23200921G= , CM000678.1:g.23200921G= | GRCh37 |
| NC_000016.8:g.23108422G= | NCBI36 |
| NG_011909.1:g.11882G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001039.4:c.547G= MANE Select | NP_001030.2:p.Gly183= |
| ENST00000300061.3:c.547G= MANE Select | ENSP00000300061.2:p.Gly183= |
| NM_001039.3:c.547G= | NP_001030.2:p.Gly183= |
| ENST00000300061.2:c.547G= | ENSP00000300061.2:p.Gly183= |