Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.72122450C= , CM000679.2:g.72122450C= | GRCh38 |
| NC_000017.10:g.70118591C= , CM000679.1:g.70118591C= | GRCh37 |
| NC_000017.9:g.67630186C= | NCBI36 |
| NG_012490.1:g.6431C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000245479.3:c.432-269C= MANE Select | ENSP00000245479.2:n.432-269C= | |
| ENST00000245479.2:c.432-269C= | ENSP00000245479.2:n.432-269C= | |
| NM_000346.3:c.432-269C= | NP_000337.1:n.432-269C= | |
| NM_000346.4:c.432-269C= MANE Select | NP_000337.1:n.432-269C= |