Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8072841C>A , CM000679.2:g.8072841C>A | GRCh38 |
| NC_000017.10:g.7976159C>A , CM000679.1:g.7976159C>A | GRCh37 |
| NC_000017.9:g.7916884C>A | NCBI36 |
| NG_007099.1:g.19863G>T | |
| NG_007099.2:g.19876G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001139.3:c.2036G>T MANE Select | NP_001130.1:p.Arg679Leu |
| ENST00000647874.1:c.2036G>T MANE Select | ENSP00000497784.1:p.Arg679Leu |
| NM_001139.2:c.2036G>T | NP_001130.1:p.Arg679Leu |
| ENST00000319144.4:c.2036G>T | ENSP00000315167.4:p.Arg679Leu |
| ENST00000649809.1:c.1100G>T | ENSP00000496845.1:p.Arg367Leu |
| ENST00000650441.1:n.459G>T |