Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110913324C= , CM000674.2:g.110913324C= | GRCh38 |
| NC_000012.11:g.111351128C= , CM000674.1:g.111351128C= | GRCh37 |
| NC_000012.10:g.109835511C= | NCBI36 |
| NG_007554.1:g.12254G= , LRG_393:g.12254G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000432.4:c.275G= MANE Select | NP_000423.2:p.Gly92= |
| ENST00000228841.15:c.275G= MANE Select | ENSP00000228841.8:p.Gly92= |
| NM_000432.3:c.275G= , LRG_393t1:c.275G= | NP_000423.2:p.Gly92= |
| ENST00000228841.12:c.275G= | ENSP00000228841.7:p.Gly92= |
| ENST00000548438.1:c.233G= | ENSP00000447154.1:p.Gly78= |
| ENST00000549029.1:n.106G= | |
| ENST00000663220.1:c.218G= | ENSP00000499568.1:p.Gly73= |