Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.34370662T>C , CM000683.2:g.34370662T>C | GRCh38 |
| NC_000021.8:g.35742961T>C , CM000683.1:g.35742961T>C | GRCh37 |
| NC_000021.7:g.34664831T>C | NCBI36 |
| NG_008804.1:g.11639T>C , LRG_291:g.11639T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_172201.2:c.184T>C MANE Select | NP_751951.1:p.Phe62Leu |
| ENST00000290310.4:c.184T>C MANE Select | ENSP00000290310.2:p.Phe62Leu |
| NM_172201.1:c.184T>C , LRG_291t1:c.184T>C | NP_751951.1:p.Phe62Leu |
| ENST00000290310.3:c.184T>C | ENSP00000290310.2:p.Phe62Leu |
| XR_001755012.2:n.780A>G | |
| XR_001755013.2:n.659A>G | |
| XR_937683.1:n.659A>G | |
| XR_937683.2:n.659A>G | |
| XR_937684.1:n.659A>G |