Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64340263G= , CM000673.2:g.64340263G= | GRCh38 |
| NC_000011.9:g.64107735G= , CM000673.1:g.64107735G= | GRCh37 |
| NC_000011.8:g.63864311G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_032251.6:c.-4G= MANE Select | NP_115627.6:n.-4G= |
| ENST00000356786.10:c.-4G= MANE Select | ENSP00000349238.5:n.-4G= |
| NM_032251.5:c.-4G= | NP_115627.6:n.-4G= |
| ENST00000356786.9:c.-4G= | ENSP00000349238.5:n.-4G= |
| ENST00000463837.5:n.41G= | |
| XM_006718519.2:c.-4G= | XP_006718582.1:n.-4G= |
| XM_006718519.4:c.-4G= | XP_006718582.1:n.-4G= |
| XM_011544957.1:c.-4G= | XP_011543259.1:n.-4G= |
| XM_011544957.2:c.-4G= | XP_011543259.1:n.-4G= |
| XM_011544958.1:c.-4G= | XP_011543260.1:n.-4G= |
| XM_011544959.1:c.-4G= | XP_011543261.1:n.-4G= |
| XM_011544959.2:c.-4G= | XP_011543261.1:n.-4G= |
| XM_011544960.1:c.-4G= | XP_011543262.1:n.-4G= |
| XM_011544960.2:c.-4G= | XP_011543262.1:n.-4G= |
| XM_011544961.1:c.-4G= | XP_011543263.1:n.-4G= |
| XM_017017601.1:c.-4G= | XP_016873090.1:n.-4G= |
| XM_024448450.1:c.-4G= | XP_024304218.1:n.-4G= |
| XM_024448451.1:c.-4G= | XP_024304219.1:n.-4G= |
| XR_002957140.1:n.59G= | |
| XR_428944.2:n.86-185C= | |
| XR_428944.3:n.102-185C= | |
| XR_949893.1:n.66G= | |
| XR_949893.3:n.60G= | |
| XR_949894.1:n.67G= | |
| XR_949894.3:n.60G= |