Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.59845386T= , CM000673.2:g.59845386T= | GRCh38 |
| NC_000011.9:g.59612859T= , CM000673.1:g.59612859T= | GRCh37 |
| NC_000011.8:g.59369435T= | NCBI36 |
| NG_008120.1:g.5116A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005142.3:c.68A= MANE Select | NP_005133.2:p.Gln23= |
| ENST00000257248.3:c.68A= MANE Select | ENSP00000257248.2:p.Gln23= |
| NM_005142.2:c.68A= | NP_005133.2:p.Gln23= |
| ENST00000257248.2:c.68A= | ENSP00000257248.2:p.Gln23= |
| ENST00000525058.5:c.68A= | ENSP00000433196.1:p.Gln23= |
| ENST00000532070.1:n.114A= | |
| XM_011544939.1:c.68A= | XP_011543241.1:p.Gln23= |
| XM_011544939.3:c.68A= | XP_011543241.1:p.Gln23= |