Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189098753C= , CM000664.2:g.189098753C= | GRCh38 |
| NC_000002.11:g.189963479C= , CM000664.1:g.189963479C= | GRCh37 |
| NC_000002.10:g.189671724C= | NCBI36 |
| NG_011799.1:g.86127G= | |
| NG_011799.2:g.86127G= | |
| NG_011799.3:g.131549G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.376G= MANE Select | ENSP00000364000.3:p.Gly126= | |
| ENST00000649966.1:c.238G= | ENSP00000496785.1:p.Gly80= | |
| ENST00000374866.7:c.376G= | ENSP00000364000.3:p.Gly126= | |
| ENST00000618828.1:c.-255G= | ENSP00000482184.1:n.-255G= | |
| NM_000393.3:c.376G= | NP_000384.2:p.Gly126= | |
| XM_011510573.1:c.238G= | XP_011508875.1:p.Gly80= | |
| NM_000393.4:c.376G= | NP_000384.2:p.Gly126= | |
| XM_011510573.3:c.238G= | XP_011508875.1:p.Gly80= | |
| NM_000393.5:c.376G= MANE Select | NP_000384.2:p.Gly126= |