Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42404546C= , CM000679.2:g.42404546C= | GRCh38 |
| NC_000017.10:g.40556564C= , CM000679.1:g.40556564C= | GRCh37 |
| NC_000017.9:g.37810090C= | NCBI36 |
| NG_015845.1:g.23775G= | |
| NG_015845.2:g.23775G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357037.6:c.*141G= MANE Select | ENSP00000349541.4:n.*141G= | |
| ENST00000357037.5:c.*141G= | ENSP00000349541.4:n.*141G= | |
| NM_012232.5:c.*141G= | NP_036364.2:n.*141G= | |
| NM_012232.6:c.*141G= MANE Select | NP_036364.2:n.*141G= |