Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.52322047C>T , CM000676.2:g.52322047C>T | GRCh38 |
| NC_000014.8:g.52788765C>T , CM000676.1:g.52788765C>T | GRCh37 |
| NC_000014.7:g.51858515C>T | NCBI36 |
| NG_013082.1:g.12750C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000245457.6:c.844-5174C>T MANE Select | ENSP00000245457.5:n.844-5174C>T | |
| ENST00000245457.5:c.844-5174C>T | ENSP00000245457.5:n.844-5174C>T | |
| ENST00000557436.1:c.79-5174C>T | ENSP00000450933.1:n.79-5174C>T | |
| NM_000956.3:c.844-5174C>T | NP_000947.2:n.844-5174C>T | |
| NM_000956.4:c.844-5174C>T MANE Select | NP_000947.2:n.844-5174C>T |