Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.209786269G= , CM000663.2:g.209786269G= | GRCh38 |
| NC_000001.10:g.209959614G= , CM000663.1:g.209959614G= | GRCh37 |
| NC_000001.9:g.208026237G= | NCBI36 |
| NG_007081.2:g.24866C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006147.4:c.*2151C= MANE Select | NP_006138.1:n.*2151C= |
| ENST00000367021.8:c.*2151C= MANE Select | ENSP00000355988.3:n.*2151C= |
| NM_001206696.1:c.*2151C= | NP_001193625.1:n.*2151C= |
| NM_001206696.2:c.*2151C= | NP_001193625.1:n.*2151C= |
| NM_006147.3:c.*2151C= | NP_006138.1:n.*2151C= |
| ENST00000367021.7:c.*2151C= | ENSP00000355988.3:n.*2151C= |
| ENST00000542854.5:c.*2151C= | ENSP00000440532.1:n.*2151C= |
| ENST00000696133.1:c.1400+2155C= | ENSP00000512426.1:n.1400+2155C= |
| ENST00000696134.1:c.*2982C= | ENSP00000512427.1:n.*2982C= |