Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.44115728C= , CM000682.2:g.44115728C= | GRCh38 |
| NC_000020.10:g.42744368C= , CM000682.1:g.42744368C= | GRCh37 |
| NC_000020.9:g.42177782C= | NCBI36 |
| NG_031867.1:g.76851G= , LRG_394:g.76851G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372980.4:c.1947G= MANE Select | ENSP00000362071.3:p.Gly649= | |
| ENST00000372980.3:c.1947G= | ENSP00000362071.3:p.Gly649= | |
| NM_020433.4:c.1947G= , LRG_394t1:c.1947G= | NP_065166.2:p.Gly649= | |
| XM_006723832.2:c.1947G= | XP_006723895.1:p.Gly649= | |
| NM_020433.5:c.1947G= MANE Select | NP_065166.2:p.Gly649= |