Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.34370662T>G , CM000683.2:g.34370662T>G | GRCh38 |
| NC_000021.8:g.35742961T>G , CM000683.1:g.35742961T>G | GRCh37 |
| NC_000021.7:g.34664831T>G | NCBI36 |
| NG_008804.1:g.11639T>G , LRG_291:g.11639T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_172201.2:c.184T>G MANE Select | NP_751951.1:p.Phe62Val |
| ENST00000290310.4:c.184T>G MANE Select | ENSP00000290310.2:p.Phe62Val |
| NM_172201.1:c.184T>G , LRG_291t1:c.184T>G | NP_751951.1:p.Phe62Val |
| ENST00000290310.3:c.184T>G | ENSP00000290310.2:p.Phe62Val |
| XR_001755012.2:n.780A>C | |
| XR_001755013.2:n.659A>C | |
| XR_937683.1:n.659A>C | |
| XR_937683.2:n.659A>C | |
| XR_937684.1:n.659A>C |