Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.51746419A= , CM000681.2:g.51746419A= | GRCh38 |
| NC_000019.9:g.52249672A= , CM000681.1:g.52249672A= | GRCh37 |
| NC_000019.8:g.56941484A= | NCBI36 |
| NG_023426.1:g.10479T= , LRG_146:g.10479T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002029.4:c.576T= MANE Select | NP_002020.1:p.Asn192= |
| ENST00000304748.5:c.576T= MANE Select | ENSP00000302707.3:p.Asn192= |
| NM_001193306.1:c.576T= | NP_001180235.1:p.Asn192= |
| NM_001193306.2:c.576T= | NP_001180235.1:p.Asn192= |
| NM_002029.3:c.576T= , LRG_146t1:c.576T= | NP_002020.1:p.Asn192= |
| ENST00000304748.4:c.576T= | ENSP00000302707.3:p.Asn192= |
| ENST00000594900.2:c.576T= | ENSP00000470750.2:p.Asn192= |
| ENST00000595042.5:c.576T= | ENSP00000471493.1:p.Asn192= |
| ENST00000600815.2:c.576T= | ENSP00000472936.2:p.Asn192= |