Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189050442G= , CM000664.2:g.189050442G= | GRCh38 |
| NC_000002.11:g.189915168G= , CM000664.1:g.189915168G= | GRCh37 |
| NC_000002.10:g.189623413G= | NCBI36 |
| NG_011799.1:g.134438C= | |
| NG_011799.2:g.134438C= | |
| NG_011799.3:g.179860C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.3039+127C= MANE Select | ENSP00000364000.3:n.3039+127C= | |
| ENST00000374866.7:c.3039+127C= | ENSP00000364000.3:n.3039+127C= | |
| ENST00000618828.1:c.1878+127C= | ENSP00000482184.1:n.1878+127C= | |
| NM_000393.3:c.3039+127C= | NP_000384.2:n.3039+127C= | |
| XM_011510573.1:c.2901+127C= | XP_011508875.1:n.2901+127C= | |
| NM_000393.4:c.3039+127C= | NP_000384.2:n.3039+127C= | |
| XM_011510573.3:c.2901+127C= | XP_011508875.1:n.2901+127C= | |
| NM_000393.5:c.3039+127C= MANE Select | NP_000384.2:n.3039+127C= |