Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31779682A>G , CM000668.2:g.31779682A>G | GRCh38 |
| NC_000006.11:g.31747459A>G , CM000668.1:g.31747459A>G | GRCh37 |
| NC_000006.10:g.31855438A>G | NCBI36 |
| NG_028229.1:g.21254T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006295.3:c.3214T>C MANE Select | NP_006286.1:p.Phe1072Leu |
| ENST00000375663.8:c.3214T>C MANE Select | ENSP00000364815.3:p.Phe1072Leu |
| NM_006295.2:c.3214T>C | NP_006286.1:p.Phe1072Leu |
| ENST00000375663.7:c.3214T>C | ENSP00000364815.3:p.Phe1072Leu |
| ENST00000463184.1:n.370T>C | |
| XM_005249362.2:c.3217T>C | XP_005249419.1:p.Phe1073Leu |
| XM_011514845.1:c.1468T>C | XP_011513147.1:p.Phe490Leu |
| XM_017011246.1:c.1468T>C | XP_016866735.1:p.Phe490Leu |
| XM_024446537.1:c.1468T>C | XP_024302305.1:p.Phe490Leu |