Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67932054C= , CM000666.2:g.67932054C= | GRCh38 |
| NC_000004.11:g.68797772C= , CM000666.1:g.68797772C= | GRCh37 |
| NC_000004.10:g.68480367C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000508048.6:c.259G= MANE Select | ENSP00000426911.2:p.Glu87= | |
| ENST00000334830.11:c.268G= | ENSP00000334611.7:p.Glu90= | |
| ENST00000396188.3:c.259G= | ENSP00000379491.3:p.Glu87= | |
| ENST00000508048.5:c.259G= | ENSP00000426911.2:p.Glu87= | |
| ENST00000513536.5:c.199G= | ENSP00000427621.1:p.Glu67= | |
| NM_001114387.1:c.259G= | NP_001107859.1:p.Glu87= | |
| NM_182606.3:c.268G= | NP_872412.3:p.Glu90= | |
| NM_001114387.2:c.259G= MANE Select | NP_001107859.1:p.Glu87= | |
| NM_182606.4:c.268G= | NP_872412.3:p.Glu90= |