Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.20778493G= , CM000686.2:g.20778493G= | GRCh38 |
| NC_000024.9:g.22940379G= , CM000686.1:g.22940379G= | GRCh37 |
| NC_000024.8:g.21349767G= | NCBI36 |
| NG_032924.1:g.27426G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000629237.2:c.533-1016G= MANE Select | ENSP00000486252.1:n.533-1016G= | |
| ENST00000629237.1:c.533-1016G= | ENSP00000486252.1:n.533-1016G= | |
| NM_001039567.2:c.533-1016G= | NP_001034656.1:n.533-1016G= | |
| XM_011531423.1:c.482-1016G= | XP_011529725.1:n.482-1016G= | |
| NM_001039567.3:c.533-1016G= MANE Select | NP_001034656.1:n.533-1016G= |