Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.155022503C= , CM000685.2:g.155022503C= | GRCh38 |
| NC_000023.10:g.154250778C= , CM000685.1:g.154250778C= | GRCh37 |
| NC_000023.9:g.153903972C= | NCBI36 |
| NG_011403.1:g.5221G= | |
| NG_011403.2:g.5221G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.50G= MANE Select | ENSP00000353393.4:p.Cys17= | |
| ENST00000647125.1:c.50G= | ENSP00000496062.1:p.Cys17= | |
| ENST00000360256.8:c.50G= | ENSP00000353393.4:p.Cys17= | |
| ENST00000423959.5:c.38+4277G= | ENSP00000409446.1:n.38+4277G= | |
| ENST00000453950.1:c.39-7G= | ENSP00000389153.1:n.39-7G= | |
| NM_000132.3:c.50G= | NP_000123.1:p.Cys17= | |
| XM_011531126.1:c.38+4277G= | XP_011529428.1:n.38+4277G= | |
| NM_000132.4:c.50G= MANE Select | NP_000123.1:p.Cys17= |