Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.42929009G= , CM000663.2:g.42929009G= | GRCh38 |
| NC_000001.10:g.43394680G= , CM000663.1:g.43394680G= | GRCh37 |
| NC_000001.9:g.43167267G= | NCBI36 |
| NG_008232.1:g.35168C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000426263.10:c.997C= MANE Select | ENSP00000416293.2:p.Arg333= | |
| ENST00000674545.1:n.491C= | ||
| ENST00000674765.1:c.997C= | ENSP00000501811.1:p.Arg333= | |
| ENST00000675112.1:n.1298C= | ||
| ENST00000676254.1:n.1446C= | ||
| ENST00000426263.7:c.997C= | ENSP00000416293.2:p.Arg333= | |
| ENST00000475162.3:c.415+1617C= | ||
| ENST00000630287.2:c.*312C= | ENSP00000486694.1:n.*312C= | |
| NM_006516.2:c.997C= | NP_006507.2:p.Arg333= | |
| NM_006516.3:c.997C= | NP_006507.2:p.Arg333= | |
| NM_006516.4:c.997C= MANE Select | NP_006507.2:p.Arg333= |