Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.96301512G>A , CM000664.2:g.96301512G>A | GRCh38 |
| NC_000002.11:g.96967250G>A , CM000664.1:g.96967250G>A | GRCh37 |
| NC_000002.10:g.96330977G>A | NCBI36 |
| NG_016973.1:g.9048C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014014.5:c.574+12C>T MANE Select | NP_054733.2:n.574+12C>T |
| ENST00000323853.10:c.574+12C>T MANE Select | ENSP00000317123.5:n.574+12C>T |
| NM_014014.4:c.574+12C>T | NP_054733.2:n.574+12C>T |
| ENST00000323853.9:c.574+12C>T | ENSP00000317123.5:n.574+12C>T |
| ENST00000652267.1:c.574+12C>T | ENSP00000498933.1:n.574+12C>T |