Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149981846T= , CM000667.2:g.149981846T= | GRCh38 |
| NC_000005.9:g.149361409T= , CM000667.1:g.149361409T= | GRCh37 |
| NC_000005.8:g.149341602T= | NCBI36 |
| NG_007147.2:g.22964T= , LRG_684:g.22964T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286298.5:c.*33T= MANE Select | ENSP00000286298.4:n.*33T= | |
| ENST00000286298.4:c.*33T= | ENSP00000286298.4:n.*33T= | |
| ENST00000503336.1:c.372+3495T= | ENSP00000426053.1:n.372+3495T= | |
| NM_000112.3:c.*33T= , LRG_684t1:c.*33T= | NP_000103.2:n.*33T= | |
| XM_017009191.2:c.*12+21T= | XP_016864680.1:n.*12+21T= | |
| NM_000112.4:c.*33T= MANE Select | NP_000103.2:n.*33T= |