Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52447749T= , CM000674.2:g.52447749T= | GRCh38 |
| NC_000012.11:g.52841533T= , CM000674.1:g.52841533T= | GRCh37 |
| NC_000012.10:g.51127800T= | NCBI36 |
| NG_008299.1:g.9378A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000252252.4:c.1424+29A= MANE Select | ENSP00000252252.3:n.1424+29A= | |
| ENST00000252252.3:c.1424+29A= | ENSP00000252252.3:n.1424+29A= | |
| NM_005555.3:c.1424+29A= | NP_005546.2:n.1424+29A= | |
| NM_005555.4:c.1424+29A= MANE Select | NP_005546.2:n.1424+29A= |