Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.54650624G= , CM000682.2:g.54650624G= | GRCh38 |
| NC_000020.10:g.53267163G= , CM000682.1:g.53267163G= | GRCh37 |
| NC_000020.9:g.52700570G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262593.10:c.*145G= MANE Select | ENSP00000262593.5:n.*145G= | |
| ENST00000262593.9:c.*145G= | ENSP00000262593.5:n.*145G= | |
| ENST00000395939.5:c.*145G= | ENSP00000379270.1:n.*145G= | |
| NM_018431.4:c.*145G= | NP_060901.2:n.*145G= | |
| NM_177959.2:c.*145G= | NP_808874.1:n.*145G= | |
| XM_011528903.1:c.*145G= | XP_011527205.1:n.*145G= | |
| XM_011528904.1:c.*145G= | XP_011527206.1:n.*145G= | |
| XM_024451946.1:c.*145G= | XP_024307714.1:n.*145G= | |
| NM_018431.5:c.*145G= MANE Select | NP_060901.2:n.*145G= | |
| NM_177959.3:c.*145G= | NP_808874.1:n.*145G= |