Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149980305T= , CM000667.2:g.149980305T= | GRCh38 |
| NC_000005.9:g.149359868T= , CM000667.1:g.149359868T= | GRCh37 |
| NC_000005.8:g.149340061T= | NCBI36 |
| NG_007147.2:g.21423T= , LRG_684:g.21423T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286298.5:c.712T= MANE Select | ENSP00000286298.4:p.Phe238= | |
| ENST00000286298.4:c.712T= | ENSP00000286298.4:p.Phe238= | |
| ENST00000503336.1:c.372+1954T= | ENSP00000426053.1:n.372+1954T= | |
| NM_000112.3:c.712T= , LRG_684t1:c.712T= | NP_000103.2:p.Phe238= | |
| XM_017009191.2:c.712T= | XP_016864680.1:p.Phe238= | |
| NM_000112.4:c.712T= MANE Select | NP_000103.2:p.Phe238= |