Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.44275636C= , CM000673.2:g.44275636C= | GRCh38 |
| NC_000011.9:g.44297186C= , CM000673.1:g.44297186C= | GRCh37 |
| NC_000011.8:g.44253762C= | NCBI36 |
| NG_015809.1:g.39531G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000652299.1:c.489G= MANE Select | ENSP00000498217.1:p.Glu163= | |
| ENST00000329255.3:c.489G= | ENSP00000332744.3:p.Glu163= | |
| NM_021926.3:c.489G= | NP_068745.2:p.Glu163= | |
| XM_011520264.1:c.489G= | XP_011518566.1:p.Glu163= | |
| XM_011520265.1:c.-34G= | XP_011518567.1:n.-34G= | |
| XM_011520266.1:c.-34G= | XP_011518568.1:n.-34G= | |
| NM_021926.4:c.489G= MANE Select | NP_068745.2:p.Glu163= |