Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1535599T>G , CM000663.2:g.1535599T>G | GRCh38 |
| NC_000001.10:g.1470979T>G , CM000663.1:g.1470979T>G | GRCh37 |
| NC_000001.9:g.1460842T>G | NCBI36 |
| NG_041807.1:g.9762A>C | |
| NG_053035.1:g.28457T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378733.9:c.363A>C MANE Select | ENSP00000368007.4:p.Gly121= | |
| ENST00000378733.8:c.363A>C | ENSP00000368007.4:p.Gly121= | |
| ENST00000425828.1:c.363A>C | ENSP00000400311.1:p.Gly121= | |
| NM_001114748.1:c.363A>C | NP_001108220.1:p.Gly121= | |
| NM_001114748.2:c.363A>C MANE Select | NP_001108220.1:p.Gly121= |