Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.70174980G= , CM000679.2:g.70174980G= | GRCh38 |
| NC_000017.10:g.68171121G= , CM000679.1:g.68171121G= | GRCh37 |
| NC_000017.9:g.65682716G= | NCBI36 |
| NG_008798.1:g.10446G= , LRG_328:g.10446G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243457.4:c.-60G= MANE Select | ENSP00000243457.2:n.-60G= | |
| ENST00000243457.3:c.-60G= | ENSP00000243457.2:n.-60G= | |
| ENST00000535240.1:c.-60G= | ENSP00000441848.1:n.-60G= | |
| NM_000891.2:c.-60G= , LRG_328t1:c.-60G= | NP_000882.1:n.-60G= | |
| XM_011524779.1:c.-60G= | XP_011523081.1:n.-60G= | |
| NM_000891.3:c.-60G= MANE Select | NP_000882.1:n.-60G= |