Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.114674204G>C , CM000674.2:g.114674204G>C | GRCh38 |
| NC_000012.11:g.115112009G>C , CM000674.1:g.115112009G>C | GRCh37 |
| NC_000012.10:g.113596392G>C | NCBI36 |
| NG_008315.1:g.14961C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349155.7:c.1671C>G MANE Select | ENSP00000257567.2:p.Thr557= | |
| ENST00000257566.7:c.1731C>G | ENSP00000257566.3:p.Thr577= | |
| ENST00000349155.6:c.1671C>G | ENSP00000257567.2:p.Thr557= | |
| ENST00000613550.1:c.1671C>G | ENSP00000480048.1:p.Thr557= | |
| NM_005996.3:c.1671C>G | NP_005987.3:p.Thr557= | |
| NM_016569.3:c.1731C>G | NP_057653.3:p.Thr577= | |
| NM_005996.4:c.1671C>G MANE Select | NP_005987.3:p.Thr557= | |
| NM_016569.4:c.1731C>G | NP_057653.3:p.Thr577= |