Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52027921T= , CM000666.2:g.52027921T= | GRCh38 |
| NC_000004.11:g.52894087T= , CM000666.1:g.52894087T= | GRCh37 |
| NC_000004.10:g.52588844T= | NCBI36 |
| NG_008891.1:g.15399A= , LRG_204:g.15399A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.753+47A= MANE Select | ENSP00000370839.6:n.753+47A= | |
| ENST00000381431.9:c.753+47A= | ENSP00000370839.5:n.753+47A= | |
| NM_000232.4:c.753+47A= , LRG_204t1:c.753+47A= | NP_000223.1:n.753+47A= | |
| XM_006714049.2:c.456+47A= | XP_006714112.1:n.456+47A= | |
| XM_011534403.1:c.543+47A= | XP_011532705.1:n.543+47A= | |
| XM_011534404.1:c.456+47A= | XP_011532706.1:n.456+47A= | |
| NM_000232.5:c.753+47A= MANE Select | NP_000223.1:n.753+47A= |