Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8076210G>A , CM000679.2:g.8076210G>A | GRCh38 |
| NC_000017.10:g.7979528G>A , CM000679.1:g.7979528G>A | GRCh37 |
| NC_000017.9:g.7920253G>A | NCBI36 |
| NG_007099.1:g.16494C>T | |
| NG_007099.2:g.16507C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001139.3:c.1497C>T MANE Select | NP_001130.1:p.Arg499= |
| ENST00000647874.1:c.1497C>T MANE Select | ENSP00000497784.1:p.Arg499= |
| NM_001139.2:c.1497C>T | NP_001130.1:p.Arg499= |
| ENST00000319144.4:c.1497C>T | ENSP00000315167.4:p.Arg499= |
| ENST00000577351.5:n.444C>T | |
| ENST00000649809.1:c.561C>T | ENSP00000496845.1:p.Arg187= |