Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102835277C= , CM000672.2:g.102835277C= | GRCh38 |
| NC_000010.10:g.104595034C= , CM000672.1:g.104595034C= | GRCh37 |
| NC_000010.9:g.104585024C= | NCBI36 |
| NG_007955.1:g.7257G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369887.4:c.413G= MANE Select | ENSP00000358903.3:p.Gly138= | |
| ENST00000638190.1:c.413G= | ENSP00000492539.1:p.Gly138= | |
| ENST00000638272.1:c.297+1788G= | ENSP00000491508.1:n.297+1788G= | |
| ENST00000638971.1:c.413G= | ENSP00000492313.1:p.Gly138= | |
| ENST00000639393.1:c.413G= | ENSP00000492651.1:p.Gly138= | |
| ENST00000640633.1:n.175G= | ||
| ENST00000369887.3:c.413G= | ENSP00000358903.3:p.Gly138= | |
| ENST00000489268.1:n.667G= | ||
| NM_000102.3:c.413G= | NP_000093.1:p.Gly138= | |
| NM_000102.4:c.413G= MANE Select | NP_000093.1:p.Gly138= |