Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.914504C>T , CM000667.2:g.914504C>T | GRCh38 |
| NC_000005.9:g.914619C>T , CM000667.1:g.914619C>T | GRCh37 |
| NC_000005.8:g.967619C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000166345.8:c.1060C>T MANE Select | ENSP00000166345.3:p.Arg354Ter | |
| ENST00000166345.7:c.1060C>T | ENSP00000166345.3:p.Arg354Ter | |
| NM_004237.3:c.1060C>T | NP_004228.1:p.Arg354Ter | |
| XM_011514163.1:c.1060C>T | XP_011512465.1:p.Arg354Ter | |
| XM_011514163.2:c.1060C>T | XP_011512465.1:p.Arg354Ter | |
| NM_004237.4:c.1060C>T MANE Select | NP_004228.1:p.Arg354Ter |