Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.43546884C= , CM000681.2:g.43546884C= | GRCh38 |
| NC_000019.9:g.44051036C= , CM000681.1:g.44051036C= | GRCh37 |
| NC_000019.8:g.48742876C= | NCBI36 |
| NG_033799.1:g.33695G= , LRG_784:g.33695G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006297.3:c.1293G= MANE Select | NP_006288.2:p.Lys431= |
| ENST00000262887.10:c.1293G= MANE Select | ENSP00000262887.5:p.Lys431= |
| NM_006297.2:c.1293G= , LRG_784t1:c.1293G= | NP_006288.2:p.Lys431= |
| ENST00000262887.9:c.1293G= | ENSP00000262887.4:p.Lys431= |
| ENST00000543982.5:c.1200G= | ENSP00000443671.1:p.Lys400= |