Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149981774A>T , CM000667.2:g.149981774A>T | GRCh38 |
| NC_000005.9:g.149361337A>T , CM000667.1:g.149361337A>T | GRCh37 |
| NC_000005.8:g.149341530A>T | NCBI36 |
| NG_007147.2:g.22892A>T , LRG_684:g.22892A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000112.4:c.2181A>T MANE Select | NP_000103.2:p.Gly727= |
| ENST00000286298.5:c.2181A>T MANE Select | ENSP00000286298.4:p.Gly727= |
| NM_000112.3:c.2181A>T , LRG_684t1:c.2181A>T | NP_000103.2:p.Gly727= |
| ENST00000286298.4:c.2181A>T | ENSP00000286298.4:p.Gly727= |
| ENST00000503336.1:c.372+3423A>T | ENSP00000426053.1:n.372+3423A>T |
| XM_017009191.2:c.2181A>T | XP_016864680.1:p.Gly727= |