Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64246639A>C , CM000673.2:g.64246639A>C | GRCh38 |
| NC_000011.9:g.64014111A>C , CM000673.1:g.64014111A>C | GRCh37 |
| NC_000011.8:g.63770687A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_138689.3:c.35T>G (PPP1R14B) MANE Select | NP_619634.1:p.Leu12Trp |
| ENST00000309318.8:c.35T>G (PPP1R14B) MANE Select | ENSP00000310117.3:p.Leu12Trp |
| NM_138689.2:c.35T>G (PPP1R14B) | NP_619634.1:p.Leu12Trp |
| NR_135087.1:n.224+550A>C (PPP1R14B-AS1) | |
| ENST00000309318.7:c.35T>G (PPP1R14B) | ENSP00000310117.3:p.Leu12Trp |
| XR_950189.1:n.195+391A>C (PPP1R14B-AS1) | |
| XR_950190.1:n.713+550A>C (PPP1R14B-AS1) |