Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116821618C>G , CM000673.2:g.116821618C>G | GRCh38 |
| NC_000011.9:g.116692334C>G , CM000673.1:g.116692334C>G | GRCh37 |
| NC_000011.8:g.116197544C>G | NCBI36 |
| NG_012044.1:g.6678G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000482.4:c.440G>C MANE Select | NP_000473.2:p.Ser147Thr |
| ENST00000357780.5:c.440G>C MANE Select | ENSP00000350425.3:p.Ser147Thr |
| NM_000482.3:c.440G>C | NP_000473.2:p.Ser147Thr |
| ENST00000357780.4:c.440G>C | ENSP00000350425.3:p.Ser147Thr |