Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.43551607T= , CM000681.2:g.43551607T= | GRCh38 |
| NC_000019.9:g.44055759T= , CM000681.1:g.44055759T= | GRCh37 |
| NC_000019.8:g.48747599T= | NCBI36 |
| NG_033799.1:g.28972A= , LRG_784:g.28972A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262887.10:c.1163A= MANE Select | ENSP00000262887.5:p.Asp388= | |
| ENST00000262887.9:c.1163A= | ENSP00000262887.4:p.Asp388= | |
| ENST00000543982.5:c.1070A= | ENSP00000443671.1:p.Asp357= | |
| ENST00000597811.5:c.773A= | ||
| NM_006297.2:c.1163A= , LRG_784t1:c.1163A= | NP_006288.2:p.Asp388= | |
| NM_006297.3:c.1163A= MANE Select | NP_006288.2:p.Asp388= |