Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52651577A>G , CM000674.2:g.52651577A>G | GRCh38 |
| NC_000012.11:g.53045361A>G , CM000674.1:g.53045361A>G | GRCh37 |
| NC_000012.10:g.51331628A>G | NCBI36 |
| NG_008296.1:g.5599T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309680.4:c.566T>C MANE Select | ENSP00000310861.3:p.Phe189Ser | |
| ENST00000309680.3:c.566T>C | ENSP00000310861.3:p.Phe189Ser | |
| NM_000423.2:c.566T>C | NP_000414.2:p.Phe189Ser | |
| NM_000423.3:c.566T>C MANE Select | NP_000414.2:p.Phe189Ser |