Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47284587G= , CM000679.2:g.47284587G= | GRCh38 |
| NC_000017.10:g.45361953G= , CM000679.1:g.45361953G= | GRCh37 |
| NC_000017.9:g.42716952G= | NCBI36 |
| NG_008332.2:g.35746G= , LRG_481:g.35746G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000212.3:c.506G= MANE Select | NP_000203.2:p.Arg169= |
| ENST00000559488.7:c.506G= MANE Select | ENSP00000452786.2:p.Arg169= |
| NM_000212.2:c.506G= , LRG_481t1:c.506G= | NP_000203.2:p.Arg169= |
| ENST00000559488.5:c.506G= | ENSP00000452786.1:p.Arg169= |
| ENST00000560629.1:c.471G= | |
| ENST00000571680.1:c.506G= | ENSP00000461626.1:p.Arg169= |
| ENST00000696963.1:c.506G= | ENSP00000513002.1:p.Arg169= |