Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94423084G= , CM000669.2:g.94423084G= | GRCh38 |
| NC_000007.13:g.94052396G= , CM000669.1:g.94052396G= | GRCh37 |
| NC_000007.12:g.93890332G= | NCBI36 |
| NG_007405.1:g.33524G= , LRG_2:g.33524G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.2531G= MANE Select | ENSP00000297268.6:p.Gly844= | |
| ENST00000297268.10:c.2531G= | ENSP00000297268.6:p.Gly844= | |
| ENST00000481570.5:n.614G= | ||
| ENST00000497316.5:n.928G= | ||
| ENST00000620463.1:c.2525G= | ENSP00000477719.1:p.Gly842= | |
| NM_000089.3:c.2531G= , LRG_2t1:c.2531G= | NP_000080.2:p.Gly844= | |
| NM_000089.4:c.2531G= MANE Select | NP_000080.2:p.Gly844= |