Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.72189927G= , CM000673.2:g.72189927G= | GRCh38 |
| NC_000011.9:g.71900971G= , CM000673.1:g.71900971G= | GRCh37 |
| NC_000011.8:g.71578619G= | NCBI36 |
| NG_015863.1:g.5370G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000312293.9:c.-9+168G= | ENSP00000308137.4:n.-9+168G= | |
| ENST00000675784.1:c.-13G= | ENSP00000502440.1:n.-13G= | |
| ENST00000312293.8:c.-9+168G= | ENSP00000308137.4:n.-9+168G= | |
| ENST00000393681.6:c.-75+168G= | ENSP00000377286.2:n.-75+168G= | |
| NM_000802.3:c.-13G= | NP_000793.1:n.-13G= | |
| NM_016724.2:c.-75+168G= | NP_057936.1:n.-75+168G= | |
| NM_016725.2:c.-9+168G= | NP_057937.1:n.-9+168G= | |
| NM_016724.3:c.-75+168G= | NP_057936.1:n.-75+168G= | |
| NM_016725.3:c.-9+168G= | NP_057937.1:n.-9+168G= |