Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.76992000G= , CM000675.2:g.76992000G= | GRCh38 |
| NC_000013.10:g.77566135G= , CM000675.1:g.77566135G= | GRCh37 |
| NC_000013.9:g.76464136G= | NCBI36 |
| NG_009064.1:g.5077G= , LRG_692:g.5077G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636183.2:c.-99G= | ENSP00000490181.2:n.-99G= | |
| ENST00000377453.7:c.49G= | ENSP00000366673.3:p.Gly17= | |
| NM_006493.2:c.49G= , LRG_692t1:c.49G= | NP_006484.1:p.Gly17= | |
| XM_011534917.1:c.49G= | XP_011533219.1:p.Gly17= |