Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149980904T= , CM000667.2:g.149980904T= | GRCh38 |
| NC_000005.9:g.149360467T= , CM000667.1:g.149360467T= | GRCh37 |
| NC_000005.8:g.149340660T= | NCBI36 |
| NG_007147.2:g.22022T= , LRG_684:g.22022T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000112.4:c.1311T= MANE Select | NP_000103.2:p.Ser437= |
| ENST00000286298.5:c.1311T= MANE Select | ENSP00000286298.4:p.Ser437= |
| NM_000112.3:c.1311T= , LRG_684t1:c.1311T= | NP_000103.2:p.Ser437= |
| ENST00000286298.4:c.1311T= | ENSP00000286298.4:p.Ser437= |
| ENST00000503336.1:c.372+2553T= | ENSP00000426053.1:n.372+2553T= |
| XM_017009191.2:c.1311T= | XP_016864680.1:p.Ser437= |