Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6077501A= , CM000674.2:g.6077501A= | GRCh38 |
| NC_000012.11:g.6186667A= , CM000674.1:g.6186667A= | GRCh37 |
| NC_000012.10:g.6056928A= | NCBI36 |
| NG_009072.1:g.52170T= | |
| NG_009072.2:g.52170T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000552.5:c.658-1950T= MANE Select | NP_000543.3:n.658-1950T= |
| ENST00000261405.10:c.658-1950T= MANE Select | ENSP00000261405.5:n.658-1950T= |
| NM_000552.3:c.658-1950T= | NP_000543.2:n.658-1950T= |
| NM_000552.4:c.658-1950T= | NP_000543.2:n.658-1950T= |
| ENST00000261405.9:c.658-1950T= | ENSP00000261405.5:n.658-1950T= |
| ENST00000538635.5:n.420+33014T= |