Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.87259754T>C , CM000665.2:g.87259754T>C | GRCh38 |
| NC_000003.11:g.87308904T>C , CM000665.1:g.87308904T>C | GRCh37 |
| NC_000003.10:g.87391594T>C | NCBI36 |
| NG_008225.2:g.21834A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344265.8:c.*140A>G | ENSP00000342931.3:n.*140A>G | |
| ENST00000350375.7:c.*140A>G MANE Select | ENSP00000263781.2:n.*140A>G | |
| ENST00000344265.7:c.*140A>G | ENSP00000342931.3:n.*140A>G | |
| ENST00000350375.6:c.*140A>G | ENSP00000263781.2:n.*140A>G | |
| NM_000306.3:c.*140A>G | NP_000297.1:n.*140A>G | |
| NM_001122757.2:c.*140A>G | NP_001116229.1:n.*140A>G | |
| NM_000306.4:c.*140A>G MANE Select | NP_000297.1:n.*140A>G | |
| NM_001122757.3:c.*140A>G | NP_001116229.1:n.*140A>G |