Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6390463G= , CM000673.2:g.6390463G= | GRCh38 |
| NC_000011.9:g.6411693G= , CM000673.1:g.6411693G= | GRCh37 |
| NC_000011.8:g.6368269G= | NCBI36 |
| NG_011780.1:g.5039G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342245.8:c.-136G= | ENSP00000340409.4:n.-136G= | |
| ENST00000530395.1:c.-272G= | ENSP00000431479.1:n.-272G= | |
| ENST00000533196.1:n.24G= | ||
| NM_000543.4:c.-136G= | NP_000534.3:n.-136G= | |
| NM_001007593.2:c.-136G= | NP_001007594.2:n.-136G= | |
| XM_005253075.3:c.-136G= | XP_005253132.1:n.-136G= | |
| XM_011520303.1:c.-136G= | XP_011518605.1:n.-136G= | |
| XM_011520304.1:c.-136G= | XP_011518606.1:n.-136G= | |
| XR_930886.1:n.163G= | ||
| NM_001318087.1:c.-136G= | NP_001305016.1:n.-136G= | |
| NM_001318088.1:c.-1097G= | NP_001305017.1:n.-1097G= | |
| NR_027400.2:n.50G= | ||
| NR_134502.1:n.50G= |