Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.34370655G>T , CM000683.2:g.34370655G>T | GRCh38 |
| NC_000021.8:g.35742954G>T , CM000683.1:g.35742954G>T | GRCh37 |
| NC_000021.7:g.34664824G>T | NCBI36 |
| NG_008804.1:g.11632G>T , LRG_291:g.11632G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_172201.2:c.177G>T MANE Select | NP_751951.1:p.Met59Ile |
| ENST00000290310.4:c.177G>T MANE Select | ENSP00000290310.2:p.Met59Ile |
| NM_172201.1:c.177G>T , LRG_291t1:c.177G>T | NP_751951.1:p.Met59Ile |
| ENST00000290310.3:c.177G>T | ENSP00000290310.2:p.Met59Ile |
| XR_001755012.2:n.787C>A | |
| XR_001755013.2:n.666C>A | |
| XR_937683.1:n.666C>A | |
| XR_937683.2:n.666C>A | |
| XR_937684.1:n.666C>A |