Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.96298916G>T , CM000664.2:g.96298916G>T | GRCh38 |
| NC_000002.11:g.96964654G>T , CM000664.1:g.96964654G>T | GRCh37 |
| NC_000002.10:g.96328381G>T | NCBI36 |
| NG_016973.1:g.11644C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014014.5:c.781C>A MANE Select | NP_054733.2:p.Arg261= |
| ENST00000323853.10:c.781C>A MANE Select | ENSP00000317123.5:p.Arg261= |
| NM_014014.4:c.781C>A | NP_054733.2:p.Arg261= |
| ENST00000323853.9:c.781C>A | ENSP00000317123.5:p.Arg261= |
| ENST00000652267.1:c.781C>A | ENSP00000498933.1:p.Arg261= |