Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151618200T= , CM000668.2:g.151618200T= | GRCh38 |
| NC_000006.11:g.151939335T= , CM000668.1:g.151939335T= | GRCh37 |
| NC_000006.10:g.151981028T= | NCBI36 |
| NG_021198.1:g.129161T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239374.8:c.*53T= MANE Select | ENSP00000239374.6:n.*53T= | |
| ENST00000239374.7:c.*53T= | ENSP00000239374.6:n.*53T= | |
| NM_025059.3:c.*53T= | NP_079335.2:n.*53T= | |
| XM_011536147.1:c.*53T= | XP_011534449.1:n.*53T= | |
| XM_011536148.1:c.*53T= | XP_011534450.1:n.*53T= | |
| XM_011536147.2:c.*53T= | XP_011534449.1:n.*53T= | |
| XM_011536148.2:c.*53T= | XP_011534450.1:n.*53T= | |
| NM_025059.4:c.*53T= MANE Select | NP_079335.2:n.*53T= |