Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.16948932C= , CM000679.2:g.16948932C= | GRCh38 |
| NC_000017.10:g.16852246C= , CM000679.1:g.16852246C= | GRCh37 |
| NC_000017.9:g.16792971C= | NCBI36 |
| NG_007281.1:g.28157G= , LRG_120:g.28157G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261652.7:c.251G= MANE Select | ENSP00000261652.2:p.Arg84= | |
| ENST00000261652.6:c.251G= | ENSP00000261652.2:p.Arg84= | |
| ENST00000579315.5:c.251G= | ENSP00000464069.1:p.Arg84= | |
| ENST00000581616.2:n.254G= | ||
| ENST00000582931.5:n.155G= | ||
| ENST00000583789.1:c.113G= | ENSP00000462952.1:p.Arg38= | |
| ENST00000584950.5:c.113G= | ENSP00000463582.1:p.Arg38= | |
| NM_012452.2:c.251G= , LRG_120t1:c.251G= | NP_036584.1:p.Arg84= | |
| NM_012452.3:c.251G= MANE Select | NP_036584.1:p.Arg84= |