Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149978258A= , CM000667.2:g.149978258A= | GRCh38 |
| NC_000005.9:g.149357821A= , CM000667.1:g.149357821A= | GRCh37 |
| NC_000005.8:g.149338014A= | NCBI36 |
| NG_007147.2:g.19376A= , LRG_684:g.19376A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000690410.1:n.838A= | ||
| ENST00000286298.5:c.606A= MANE Select | ENSP00000286298.4:p.Thr202= | |
| ENST00000286298.4:c.606A= | ENSP00000286298.4:p.Thr202= | |
| ENST00000503336.1:c.279A= | ENSP00000426053.1:p.Thr93= | |
| NM_000112.3:c.606A= , LRG_684t1:c.606A= | NP_000103.2:p.Thr202= | |
| XM_017009191.2:c.606A= | XP_016864680.1:p.Thr202= | |
| NM_000112.4:c.606A= MANE Select | NP_000103.2:p.Thr202= |