Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.12093889G>A , CM000672.2:g.12093889G>A | GRCh38 |
| NC_000010.10:g.12135888G>A , CM000672.1:g.12135888G>A | GRCh37 |
| NC_000010.9:g.12175894G>A | NCBI36 |
| NG_033248.1:g.29973G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_018706.7:c.1160-184G>A MANE Select | NP_061176.4:n.1160-184G>A |
| ENST00000263035.9:c.1160-184G>A MANE Select | ENSP00000263035.4:n.1160-184G>A |
| NM_018706.6:c.1160-184G>A | NP_061176.3:n.1160-184G>A |
| ENST00000263035.8:c.1160-184G>A | ENSP00000263035.4:n.1160-184G>A |
| ENST00000415935.1:c.254-184G>A | ENSP00000400625.1:n.254-184G>A |
| ENST00000465617.1:n.300-184G>A |