Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55156237C= , CM000681.2:g.55156237C= | GRCh38 |
| NC_000019.9:g.55667605C= , CM000681.1:g.55667605C= | GRCh37 |
| NC_000019.8:g.60359417C= | NCBI36 |
| NG_007866.2:g.6496G= , LRG_432:g.6496G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000363.5:c.246G= MANE Select | NP_000354.4:p.Pro82= |
| ENST00000344887.10:c.246G= MANE Select | ENSP00000341838.5:p.Pro82= |
| NM_000363.4:c.246G= , LRG_432t1:c.246G= | NP_000354.4:p.Pro82= |
| ENST00000344887.9:c.246G= | ENSP00000341838.5:p.Pro82= |
| ENST00000585806.5:n.245G= | |
| ENST00000586669.5:n.254G= | |
| ENST00000587176.5:n.430G= | |
| ENST00000587871.1:c.865G= | |
| ENST00000588882.1:c.171G= | ENSP00000466729.1:p.Pro57= |
| ENST00000590463.1:n.418G= | |
| ENST00000665070.1:c.246G= | ENSP00000499482.1:p.Pro82= |