Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.842170G= , CM000671.2:g.842170G= | GRCh38 |
| NC_000009.11:g.842170G= , CM000671.1:g.842170G= | GRCh37 |
| NC_000009.10:g.832170G= | NCBI36 |
| NG_009221.1:g.5481G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_021951.3:c.332G= MANE Select | NP_068770.2:p.Arg111= |
| ENST00000382276.8:c.332G= MANE Select | ENSP00000371711.3:p.Arg111= |
| NM_021951.2:c.332G= | NP_068770.2:p.Arg111= |
| ENST00000382276.7:c.332G= | ENSP00000371711.3:p.Arg111= |
| ENST00000564322.1:n.481G= | |
| XM_006716732.1:c.332G= | XP_006716795.1:p.Arg111= |
| XM_017014375.1:c.332G= | XP_016869864.1:p.Arg111= |