Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.68231862T>C , CM000672.2:g.68231862T>C | GRCh38 |
| NC_000010.10:g.69991619T>C , CM000672.1:g.69991619T>C | GRCh37 |
| NC_000010.9:g.69661625T>C | NCBI36 |
| NG_031934.1:g.5252A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_145178.4:c.-185A>G MANE Select | NP_660161.1:n.-185A>G |
| ENST00000373673.5:c.-185A>G MANE Select | ENSP00000362777.3:n.-185A>G |
| NM_145178.3:c.-185A>G | NP_660161.1:n.-185A>G |
| ENST00000373673.4:c.-185A>G | ENSP00000362777.3:n.-185A>G |