Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.27750424T= , CM000684.2:g.27750424T= | GRCh38 |
| NC_000022.10:g.28146412T= , CM000684.1:g.28146412T= | GRCh37 |
| NC_000022.9:g.26476412T= | NCBI36 |
| NG_023258.1:g.56075A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703102.1:n.979A= | ||
| ENST00000302326.5:c.*491A= MANE Select | ENSP00000304956.4:n.*491A= | |
| ENST00000302326.4:c.*491A= | ENSP00000304956.4:n.*491A= | |
| ENST00000424656.1:c.456-196A= | ||
| NM_002430.2:c.*491A= | NP_002421.3:n.*491A= | |
| NM_002430.3:c.*491A= MANE Select | NP_002421.3:n.*491A= |