Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.74743905G>A , CM000685.2:g.74743905G>A | GRCh38 |
| NC_000023.10:g.73963740G>A , CM000685.1:g.73963740G>A | GRCh37 |
| NC_000023.9:g.73880465G>A | NCBI36 |
| NG_027726.1:g.186548C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000055682.12:c.652C>T MANE Select | ENSP00000055682.5:p.Arg218Ter | |
| ENST00000616200.2:c.652C>T | ENSP00000480284.1:p.Arg218Ter | |
| ENST00000642681.2:c.652C>T | ENSP00000495800.1:p.Arg218Ter | |
| ENST00000055682.10:c.652C>T | ENSP00000055682.5:p.Arg218Ter | |
| ENST00000616200.1:c.652C>T | ENSP00000480284.1:p.Arg218Ter | |
| NM_001008537.2:c.652C>T | NP_001008537.1:p.Arg218Ter | |
| XM_011530935.1:c.652C>T | XP_011529237.1:p.Arg218Ter | |
| NM_001008537.3:c.652C>T MANE Select | NP_001008537.1:p.Arg218Ter |