Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149981872T= , CM000667.2:g.149981872T= | GRCh38 |
| NC_000005.9:g.149361435T= , CM000667.1:g.149361435T= | GRCh37 |
| NC_000005.8:g.149341628T= | NCBI36 |
| NG_007147.2:g.22990T= , LRG_684:g.22990T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286298.5:c.*59T= MANE Select | ENSP00000286298.4:n.*59T= | |
| ENST00000286298.4:c.*59T= | ENSP00000286298.4:n.*59T= | |
| ENST00000503336.1:c.372+3521T= | ENSP00000426053.1:n.372+3521T= | |
| NM_000112.3:c.*59T= , LRG_684t1:c.*59T= | NP_000103.2:n.*59T= | |
| XM_017009191.2:c.*12+47T= | XP_016864680.1:n.*12+47T= | |
| NM_000112.4:c.*59T= MANE Select | NP_000103.2:n.*59T= |