Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.108578080dup , CM000685.2:g.108578080dup | GRCh38 |
| NC_000023.10:g.107821310dup , CM000685.1:g.107821310dup | GRCh37 |
| NC_000023.9:g.107707966dup | NCBI36 |
| NG_011977.1:g.143157dup | |
| NG_011977.2:g.143157dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328300.11:c.648dup | ||
| ENST00000361603.7:c.648dup | ||
| ENST00000328300.10:c.648dup | ||
| ENST00000361603.6:c.648dup | ||
| NM_000495.4:c.648dup | ||
| NM_033380.2:c.648dup | ||
| XM_005262070.2:c.648dup | ||
| XM_005262072.3:c.648dup | ||
| XM_006724616.2:c.648dup | ||
| XM_011530849.1:c.324dup | ||
| XM_011530850.1:c.648dup | ||
| XM_011530849.2:c.663dup | ||
| XM_017029259.2:c.663dup | ||
| XM_017029260.1:c.663dup | ||
| XM_017029261.1:c.663dup | ||
| XM_017029262.2:c.663dup | ||
| NM_000495.5:c.648dup | ||
| NM_033380.3:c.648dup |