Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149978184C= , CM000667.2:g.149978184C= | GRCh38 |
| NC_000005.9:g.149357747C= , CM000667.1:g.149357747C= | GRCh37 |
| NC_000005.8:g.149337940C= | NCBI36 |
| NG_007147.2:g.19302C= , LRG_684:g.19302C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000112.4:c.532C= MANE Select | NP_000103.2:p.Arg178= |
| ENST00000286298.5:c.532C= MANE Select | ENSP00000286298.4:p.Arg178= |
| NM_000112.3:c.532C= , LRG_684t1:c.532C= | NP_000103.2:p.Arg178= |
| ENST00000286298.4:c.532C= | ENSP00000286298.4:p.Arg178= |
| ENST00000503336.1:c.205C= | ENSP00000426053.1:p.Arg69= |
| ENST00000690410.1:n.764C= | |
| XM_017009191.2:c.532C= | XP_016864680.1:p.Arg178= |