Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55052398G= , CM000663.2:g.55052398G= | GRCh38 |
| NC_000001.10:g.55518071G= , CM000663.1:g.55518071G= | GRCh37 |
| NC_000001.9:g.55290659G= | NCBI36 |
| NG_009061.1:g.17852G= , LRG_275:g.17852G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_174936.4:c.644G= MANE Select | NP_777596.2:p.Arg215= |
| ENST00000302118.5:c.644G= MANE Select | ENSP00000303208.5:p.Arg215= |
| NM_174936.3:c.644G= , LRG_275t1:c.644G= | NP_777596.2:p.Arg215= |
| NR_110451.1:n.303G= | |
| NR_110451.2:n.303G= | |
| ENST00000490692.1:n.1465G= | |
| ENST00000673726.1:c.*140G= | ENSP00000501004.1:n.*140G= |
| ENST00000673903.1:c.269G= | ENSP00000501257.1:p.Arg90= |
| ENST00000673913.2:c.644G= | ENSP00000501161.2:p.Arg215= |
| ENST00000710286.1:c.1001G= | ENSP00000518176.1:p.Arg334= |