Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52490844G>A , CM000674.2:g.52490844G>A | GRCh38 |
| NC_000012.11:g.52884628G>A , CM000674.1:g.52884628G>A | GRCh37 |
| NC_000012.10:g.51170895G>A | NCBI36 |
| NG_008298.1:g.7554C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005554.4:c.912+14C>T MANE Select | NP_005545.1:n.912+14C>T |
| ENST00000330722.7:c.912+14C>T MANE Select | ENSP00000369317.3:n.912+14C>T |
| NM_005554.3:c.912+14C>T | NP_005545.1:n.912+14C>T |
| ENST00000330722.6:c.912+14C>T | ENSP00000369317.3:n.912+14C>T |
| ENST00000549600.1:n.300+14C>T | |
| ENST00000549754.1:n.261+14C>T | |
| ENST00000549898.5:n.447C>T |