Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33302117C= , CM000681.2:g.33302117C= | GRCh38 |
| NC_000019.9:g.33793023C= , CM000681.1:g.33793023C= | GRCh37 |
| NC_000019.8:g.38484863C= | NCBI36 |
| NG_012022.1:g.5408G= , LRG_456:g.5408G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000498907.3:c.298G= MANE Select | ENSP00000427514.1:p.Gly100= | |
| ENST00000498907.2:c.298G= | ENSP00000427514.1:p.Gly100= | |
| NM_001285829.1:c.-60G= | NP_001272758.1:n.-60G= | |
| NM_001287424.1:c.403G= | NP_001274353.1:p.Gly135= | |
| NM_001287435.1:c.256G= | NP_001274364.1:p.Gly86= | |
| NM_004364.4:c.298G= | NP_004355.2:p.Gly100= | |
| NM_001287424.2:c.403G= | NP_001274353.1:p.Gly135= | |
| NM_004364.5:c.298G= MANE Select | NP_004355.2:p.Gly100= | |
| NM_001285829.2:c.-60G= | NP_001272758.1:n.-60G= | |
| NM_001287435.2:c.256G= | NP_001274364.1:p.Gly86= |