Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.106380080C>T , CM000674.2:g.106380080C>T | GRCh38 |
| NC_000012.11:g.106773858C>T , CM000674.1:g.106773858C>T | GRCh37 |
| NC_000012.10:g.105297988C>T | NCBI36 |
| NG_031837.1:g.27423C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_018082.6:c.664C>T MANE Select | NP_060552.4:p.Arg222Ter |
| ENST00000228347.9:c.664C>T MANE Select | ENSP00000228347.4:p.Arg222Ter |
| NM_001160708.1:c.490C>T | NP_001154180.1:p.Arg164Ter |
| NM_001160708.2:c.490C>T | NP_001154180.1:p.Arg164Ter |
| NM_018082.5:c.664C>T | NP_060552.4:p.Arg222Ter |
| ENST00000228347.8:c.664C>T | ENSP00000228347.4:p.Arg222Ter |
| ENST00000539066.5:c.490C>T | ENSP00000445721.1:p.Arg164Ter |
| XM_017019621.2:c.664C>T | XP_016875110.1:p.Arg222Ter |