Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149981128C= , CM000667.2:g.149981128C= | GRCh38 |
| NC_000005.9:g.149360691C= , CM000667.1:g.149360691C= | GRCh37 |
| NC_000005.8:g.149340884C= | NCBI36 |
| NG_007147.2:g.22246C= , LRG_684:g.22246C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000112.4:c.1535C= MANE Select | NP_000103.2:p.Thr512= |
| ENST00000286298.5:c.1535C= MANE Select | ENSP00000286298.4:p.Thr512= |
| NM_000112.3:c.1535C= , LRG_684t1:c.1535C= | NP_000103.2:p.Thr512= |
| ENST00000286298.4:c.1535C= | ENSP00000286298.4:p.Thr512= |
| ENST00000503336.1:c.372+2777C= | ENSP00000426053.1:n.372+2777C= |
| XM_017009191.2:c.1535C= | XP_016864680.1:p.Thr512= |