Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33302027C= , CM000681.2:g.33302027C= | GRCh38 |
| NC_000019.9:g.33792933C= , CM000681.1:g.33792933C= | GRCh37 |
| NC_000019.8:g.38484773C= | NCBI36 |
| NG_012022.1:g.5498G= , LRG_456:g.5498G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000498907.3:c.388G= MANE Select | ENSP00000427514.1:p.Gly130= | |
| ENST00000498907.2:c.388G= | ENSP00000427514.1:p.Gly130= | |
| NM_001285829.1:c.31G= | NP_001272758.1:p.Gly11= | |
| NM_001287424.1:c.493G= | NP_001274353.1:p.Gly165= | |
| NM_001287435.1:c.346G= | NP_001274364.1:p.Gly116= | |
| NM_004364.4:c.388G= | NP_004355.2:p.Gly130= | |
| NM_001287424.2:c.493G= | NP_001274353.1:p.Gly165= | |
| NM_004364.5:c.388G= MANE Select | NP_004355.2:p.Gly130= | |
| NM_001285829.2:c.31G= | NP_001272758.1:p.Gly11= | |
| NM_001287435.2:c.346G= | NP_001274364.1:p.Gly116= |