Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47286419T>A , CM000679.2:g.47286419T>A | GRCh38 |
| NC_000017.10:g.45363785T>A , CM000679.1:g.45363785T>A | GRCh37 |
| NC_000017.9:g.42718784T>A | NCBI36 |
| NG_008332.2:g.37578T>A , LRG_481:g.37578T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000212.3:c.774T>A MANE Select | NP_000203.2:p.Cys258Ter |
| ENST00000559488.7:c.774T>A MANE Select | ENSP00000452786.2:p.Cys258Ter |
| NM_000212.2:c.774T>A , LRG_481t1:c.774T>A | NP_000203.2:p.Cys258Ter |
| ENST00000559488.5:c.774T>A | ENSP00000452786.1:p.Cys258Ter |
| ENST00000560629.1:c.739T>A | |
| ENST00000571680.1:c.774T>A | ENSP00000461626.1:p.Cys258Ter |
| ENST00000696963.1:c.774T>A | ENSP00000513002.1:p.Cys258Ter |