Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.103458291C= , CM000672.2:g.103458291C= | GRCh38 |
| NC_000010.10:g.105218048C= , CM000672.1:g.105218048C= | GRCh37 |
| NC_000010.9:g.105208038C= | NCBI36 |
| NG_016855.1:g.5601G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001001412.4:c.461G= MANE Select | NP_001001412.3:p.Arg154= |
| ENST00000329905.6:c.461G= MANE Select | ENSP00000329926.6:p.Arg154= |
| NM_001001412.3:c.461G= | NP_001001412.3:p.Arg154= |
| ENST00000329905.5:c.461G= | ENSP00000329926.5:p.Arg154= |