Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49126485A>C , CM000665.2:g.49126485A>C | GRCh38 |
| NC_000003.11:g.49163918A>C , CM000665.1:g.49163918A>C | GRCh37 |
| NC_000003.10:g.49138922A>C | NCBI36 |
| NG_008094.1:g.11682T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002292.4:c.2031T>G MANE Select | NP_002283.3:p.Phe677Leu |
| ENST00000305544.9:c.2031T>G MANE Select | ENSP00000307156.4:p.Phe677Leu |
| NM_002292.3:c.2031T>G | NP_002283.3:p.Phe677Leu |
| ENST00000305544.8:c.2031T>G | ENSP00000307156.4:p.Phe677Leu |
| ENST00000418109.5:c.2031T>G | ENSP00000388325.1:p.Phe677Leu |
| ENST00000486298.5:n.112T>G | |
| ENST00000488638.1:n.221T>G | |
| XM_005265127.3:c.2031T>G | XP_005265184.1:p.Phe677Leu |
| XM_005265127.4:c.2031T>G | XP_005265184.1:p.Phe677Leu |