Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.209786302A= , CM000663.2:g.209786302A= | GRCh38 |
| NC_000001.10:g.209959647A= , CM000663.1:g.209959647A= | GRCh37 |
| NC_000001.9:g.208026270A= | NCBI36 |
| NG_007081.2:g.24833T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696133.1:c.1400+2122T= | ENSP00000512426.1:n.1400+2122T= | |
| ENST00000696134.1:c.*2949T= | ENSP00000512427.1:n.*2949T= | |
| ENST00000367021.8:c.*2118T= MANE Select | ENSP00000355988.3:n.*2118T= | |
| ENST00000367021.7:c.*2118T= | ENSP00000355988.3:n.*2118T= | |
| ENST00000542854.5:c.*2118T= | ENSP00000440532.1:n.*2118T= | |
| NM_001206696.1:c.*2118T= | NP_001193625.1:n.*2118T= | |
| NM_006147.3:c.*2118T= | NP_006138.1:n.*2118T= | |
| NM_006147.4:c.*2118T= MANE Select | NP_006138.1:n.*2118T= | |
| NM_001206696.2:c.*2118T= | NP_001193625.1:n.*2118T= |