Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075583C= , CM000679.2:g.8075583C= | GRCh38 |
| NC_000017.10:g.7978901C= , CM000679.1:g.7978901C= | GRCh37 |
| NC_000017.9:g.7919626C= | NCBI36 |
| NG_007099.1:g.17121G= | |
| NG_007099.2:g.17134G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.1654+12G= MANE Select | ENSP00000497784.1:n.1654+12G= | |
| ENST00000649809.1:c.718+12G= | ENSP00000496845.1:n.718+12G= | |
| ENST00000319144.4:c.1654+12G= | ENSP00000315167.4:n.1654+12G= | |
| ENST00000577351.5:n.479+592G= | ||
| NM_001139.2:c.1654+12G= | NP_001130.1:n.1654+12G= | |
| NM_001139.3:c.1654+12G= MANE Select | NP_001130.1:n.1654+12G= |