Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149981720C= , CM000667.2:g.149981720C= | GRCh38 |
| NC_000005.9:g.149361283C= , CM000667.1:g.149361283C= | GRCh37 |
| NC_000005.8:g.149341476C= | NCBI36 |
| NG_007147.2:g.22838C= , LRG_684:g.22838C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286298.5:c.2127C= MANE Select | ENSP00000286298.4:p.Phe709= | |
| ENST00000286298.4:c.2127C= | ENSP00000286298.4:p.Phe709= | |
| ENST00000503336.1:c.372+3369C= | ENSP00000426053.1:n.372+3369C= | |
| NM_000112.3:c.2127C= , LRG_684t1:c.2127C= | NP_000103.2:p.Phe709= | |
| XM_017009191.2:c.2127C= | XP_016864680.1:p.Phe709= | |
| NM_000112.4:c.2127C= MANE Select | NP_000103.2:p.Phe709= |