Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55157097G= , CM000681.2:g.55157097G= | GRCh38 |
| NC_000019.9:g.55668465G= , CM000681.1:g.55668465G= | GRCh37 |
| NC_000019.8:g.60360277G= | NCBI36 |
| NG_007866.2:g.5636C= , LRG_432:g.5636C= | |
| NG_032759.1:g.14626C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000363.5:c.61C= MANE Select | NP_000354.4:p.Arg21= |
| ENST00000344887.10:c.61C= MANE Select | ENSP00000341838.5:p.Arg21= |
| NM_000363.4:c.61C= , LRG_432t1:c.61C= | NP_000354.4:p.Arg21= |
| ENST00000344887.9:c.61C= | ENSP00000341838.5:p.Arg21= |
| ENST00000586446.1:n.203C= | |
| ENST00000586669.5:n.69C= | |
| ENST00000587176.5:n.245C= | |
| ENST00000587871.1:c.680C= | |
| ENST00000590463.1:n.233C= | |
| ENST00000665070.1:c.61C= | ENSP00000499482.1:p.Arg21= |