Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21702773C= , CM000669.2:g.21702773C= | GRCh38 |
| NC_000007.13:g.21742391C= , CM000669.1:g.21742391C= | GRCh37 |
| NC_000007.12:g.21708916C= | NCBI36 |
| NG_012886.2:g.164559C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001277115.2:c.6244C= MANE Select | NP_001264044.1:p.Arg2082= |
| ENST00000409508.8:c.6244C= MANE Select | ENSP00000475939.1:p.Arg2082= |
| NM_001277115.1:c.6244C= | NP_001264044.1:p.Arg2082= |
| ENST00000328843.10:c.6265C= | ENSP00000330671.7:p.Arg2089= |
| ENST00000409508.7:c.6244C= | ENSP00000475939.1:p.Arg2082= |
| ENST00000465129.1:n.64C= | |
| ENST00000620169.4:c.6265C= | ENSP00000481693.1:p.Arg2089= |