Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6390460G= , CM000673.2:g.6390460G= | GRCh38 |
| NC_000011.9:g.6411690G= , CM000673.1:g.6411690G= | GRCh37 |
| NC_000011.8:g.6368266G= | NCBI36 |
| NG_011780.1:g.5036G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342245.8:c.-139G= | ENSP00000340409.4:n.-139G= | |
| ENST00000530395.1:c.-275G= | ENSP00000431479.1:n.-275G= | |
| ENST00000533196.1:n.21G= | ||
| NM_000543.4:c.-139G= | NP_000534.3:n.-139G= | |
| NM_001007593.2:c.-139G= | NP_001007594.2:n.-139G= | |
| XM_005253075.3:c.-139G= | XP_005253132.1:n.-139G= | |
| XM_011520303.1:c.-139G= | XP_011518605.1:n.-139G= | |
| XM_011520304.1:c.-139G= | XP_011518606.1:n.-139G= | |
| XR_930886.1:n.160G= | ||
| NM_001318087.1:c.-139G= | NP_001305016.1:n.-139G= | |
| NM_001318088.1:c.-1100G= | NP_001305017.1:n.-1100G= | |
| NR_027400.2:n.47G= | ||
| NR_134502.1:n.47G= |