Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.111704282G= , CM000665.2:g.111704282G= | GRCh38 |
| NC_000003.11:g.111423129G= , CM000665.1:g.111423129G= | GRCh37 |
| NC_000003.10:g.112905819G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636933.2:c.164-3644G= MANE Select | ENSP00000490816.1:n.164-3644G= | |
| ENST00000477665.2:c.164-3644G= | ENSP00000420686.1:n.164-3644G= | |
| ENST00000636933.1:c.164-3644G= | ENSP00000490816.1:n.164-3644G= | |
| ENST00000393934.7:c.164-3644G= | ENSP00000377511.3:n.164-3644G= | |
| ENST00000468174.1:c.-107-3644G= | ENSP00000417436.1:n.-107-3644G= | |
| ENST00000477665.1:c.164-3644G= | ENSP00000420686.1:n.164-3644G= | |
| NM_001185106.1:c.164-3644G= | NP_001172035.1:n.164-3644G= | |
| NM_153268.3:c.164-3644G= | NP_695000.1:n.164-3644G= |