Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20189076C= , CM000675.2:g.20189076C= | GRCh38 |
| NC_000013.10:g.20763215C= , CM000675.1:g.20763215C= | GRCh37 |
| NC_000013.9:g.19661215C= | NCBI36 |
| NG_008358.1:g.8900G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382844.2:c.506G= | ENSP00000372295.1:p.Cys169= | |
| ENST00000382848.5:c.506G= MANE Select | ENSP00000372299.4:p.Cys169= | |
| ENST00000382844.1:c.506G= | ENSP00000372295.1:p.Cys169= | |
| ENST00000382848.4:c.506G= | ENSP00000372299.4:p.Cys169= | |
| NM_004004.5:c.506G= | NP_003995.2:p.Cys169= | |
| XM_011535049.1:c.506G= | XP_011533351.1:p.Cys169= | |
| XM_011535049.2:c.506G= | XP_011533351.1:p.Cys169= | |
| NM_004004.6:c.506G= MANE Select | NP_003995.2:p.Cys169= |