Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102480984A= , CM000674.2:g.102480984A= | GRCh38 |
| NC_000012.11:g.102874762A= , CM000674.1:g.102874762A= | GRCh37 |
| NC_000012.10:g.101398892A= | NCBI36 |
| NG_011713.1:g.4617T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000644491.1:c.-19-584T= | ENSP00000494228.1:n.-19-584T= |
| XM_017019259.1:c.114+719T= | XP_016874748.1:n.114+719T= |
| XM_017019262.2:c.114+719T= | XP_016874751.1:n.114+719T= |
| XM_017019263.2:c.114+719T= | XP_016874752.1:n.114+719T= |
| XR_944536.1:n.84+719T= |