Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154806G>T , CM000681.2:g.55154806G>T | GRCh38 |
| NC_000019.9:g.55666174G>T , CM000681.1:g.55666174G>T | GRCh37 |
| NC_000019.8:g.60357986G>T | NCBI36 |
| NG_007866.2:g.7927C>A , LRG_432:g.7927C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000363.5:c.307C>A MANE Select | NP_000354.4:p.Arg103Ser |
| ENST00000344887.10:c.307C>A MANE Select | ENSP00000341838.5:p.Arg103Ser |
| NM_000363.4:c.307C>A , LRG_432t1:c.307C>A | NP_000354.4:p.Arg103Ser |
| ENST00000344887.9:c.307C>A | ENSP00000341838.5:p.Arg103Ser |
| ENST00000585806.5:n.306C>A | |
| ENST00000586669.5:n.315C>A | |
| ENST00000587176.5:n.491C>A | |
| ENST00000587871.1:c.926C>A | |
| ENST00000588882.1:c.232C>A | ENSP00000466729.1:p.Arg78Ser |
| ENST00000590463.1:n.479C>A | |
| ENST00000665070.1:c.307C>A | ENSP00000499482.1:p.Arg103Ser |