Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94400213A>G , CM000669.2:g.94400213A>G | GRCh38 |
| NC_000007.13:g.94029525A>G , CM000669.1:g.94029525A>G | GRCh37 |
| NC_000007.12:g.93867461A>G | NCBI36 |
| NG_007405.1:g.10653A>G , LRG_2:g.10653A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.150A>G MANE Select | NP_000080.2:p.Pro50= |
| ENST00000297268.11:c.150A>G MANE Select | ENSP00000297268.6:p.Pro50= |
| NM_000089.3:c.150A>G , LRG_2t1:c.150A>G | NP_000080.2:p.Pro50= |
| ENST00000297268.10:c.150A>G | ENSP00000297268.6:p.Pro50= |
| ENST00000620463.1:c.144A>G | ENSP00000477719.1:p.Pro48= |