Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.41756399C= , CM000683.2:g.41756399C= | GRCh38 |
| NC_000021.8:g.43176559C= , CM000683.1:g.43176559C= | GRCh37 |
| NC_000021.7:g.42049628C= | NCBI36 |
| NG_032113.1:g.15691G= | |
| NG_032113.2:g.15691G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332512.8:c.474+126G= MANE Select | ENSP00000332454.3:n.474+126G= | |
| ENST00000332512.7:c.474+126G= | ENSP00000332454.3:n.474+126G= | |
| ENST00000352483.3:c.474+126G= | ENSP00000330161.2:n.474+126G= | |
| NM_020639.2:c.474+126G= | NP_065690.2:n.474+126G= | |
| NM_020639.3:c.474+126G= MANE Select | NP_065690.2:n.474+126G= |