Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189035184A= , CM000664.2:g.189035184A= | GRCh38 |
| NC_000002.11:g.189899910A= , CM000664.1:g.189899910A= | GRCh37 |
| NC_000002.10:g.189608155A= | NCBI36 |
| NG_011799.1:g.149696T= | |
| NG_011799.2:g.149696T= | |
| NG_011799.3:g.195118T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.4114-29T= MANE Select | ENSP00000364000.3:n.4114-29T= | |
| ENST00000374866.7:c.4114-29T= | ENSP00000364000.3:n.4114-29T= | |
| ENST00000618828.1:c.2953-29T= | ENSP00000482184.1:n.2953-29T= | |
| NM_000393.3:c.4114-29T= | NP_000384.2:n.4114-29T= | |
| XM_011510573.1:c.3976-29T= | XP_011508875.1:n.3976-29T= | |
| NM_000393.4:c.4114-29T= | NP_000384.2:n.4114-29T= | |
| XM_011510573.3:c.3976-29T= | XP_011508875.1:n.3976-29T= | |
| NM_000393.5:c.4114-29T= MANE Select | NP_000384.2:n.4114-29T= |