Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7932931C>G , CM000681.2:g.7932931C>G | GRCh38 |
| NC_000019.9:g.7997816C>G , CM000681.1:g.7997816C>G | GRCh37 |
| NC_000019.8:g.7903816C>G | NCBI36 |
| NG_051180.1:g.15893G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270538.8:c.771G>C MANE Select | ENSP00000270538.2:p.Arg257= | |
| ENST00000270538.7:c.771G>C | ENSP00000270538.2:p.Arg257= | |
| ENST00000595831.5:c.758G>C | ||
| ENST00000595876.5:c.*459G>C | ENSP00000471596.1:n.*459G>C | |
| ENST00000597926.1:c.675G>C | ENSP00000469389.1:p.Arg225= | |
| ENST00000598675.1:n.177G>C | ||
| NM_006351.3:c.771G>C | NP_006342.2:p.Arg257= | |
| NM_006351.4:c.771G>C MANE Select | NP_006342.2:p.Arg257= |