Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.172659462T>G , CM000663.2:g.172659462T>G | GRCh38 |
| NC_000001.10:g.172628602T>G , CM000663.1:g.172628602T>G | GRCh37 |
| NC_000001.9:g.170895225T>G | NCBI36 |
| NG_007269.1:g.5418T>G , LRG_58:g.5418T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000639.3:c.261T>G MANE Select | NP_000630.1:p.Phe87Leu |
| ENST00000367721.3:c.261T>G MANE Select | ENSP00000356694.2:p.Phe87Leu |
| NM_000639.2:c.261T>G | NP_000630.1:p.Phe87Leu |
| NM_001302746.1:c.261T>G | NP_001289675.1:p.Phe87Leu |
| NM_001302746.2:c.261T>G | NP_001289675.1:p.Phe87Leu |
| ENST00000340030.4:c.261T>G | ENSP00000344739.3:p.Phe87Leu |
| ENST00000367721.2:c.261T>G | ENSP00000356694.2:p.Phe87Leu |