Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.42927627C= , CM000663.2:g.42927627C= | GRCh38 |
| NC_000001.10:g.43393298C= , CM000663.1:g.43393298C= | GRCh37 |
| NC_000001.9:g.43165885C= | NCBI36 |
| NG_008232.1:g.36550G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006516.4:c.1256G= MANE Select | NP_006507.2:p.Gly419= |
| ENST00000426263.10:c.1256G= MANE Select | ENSP00000416293.2:p.Gly419= |
| NM_006516.2:c.1256G= | NP_006507.2:p.Gly419= |
| NM_006516.3:c.1256G= | NP_006507.2:p.Gly419= |
| ENST00000426263.7:c.1256G= | ENSP00000416293.2:p.Gly419= |
| ENST00000475162.3:c.416-649G= | |
| ENST00000630287.2:c.*571G= | ENSP00000486694.1:n.*571G= |
| ENST00000674545.1:n.1873G= | |
| ENST00000674765.1:c.1030-770G= | ENSP00000501811.1:n.1030-770G= |
| ENST00000675112.1:n.1557G= | |
| ENST00000676254.1:n.1705G= |