Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.64190403C>T , CM000685.2:g.64190403C>T | GRCh38 |
| NC_000023.10:g.63410283C>T , CM000685.1:g.63410283C>T | GRCh37 |
| NC_000023.9:g.63327008C>T | NCBI36 |
| NG_021345.1:g.20342G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_152424.4:c.2884G>A MANE Select | NP_689637.3:p.Ala962Thr |
| ENST00000374869.8:c.2884G>A MANE Select | ENSP00000364003.4:p.Ala962Thr |
| NM_152424.3:c.2884G>A | NP_689637.3:p.Ala962Thr |
| ENST00000330258.3:c.2884G>A | ENSP00000329117.3:p.Ala962Thr |
| ENST00000374869.7:c.2357+527G>A | ENSP00000364003.3:n.2357+527G>A |
| XM_011530858.1:c.2884G>A | XP_011529160.1:p.Ala962Thr |