Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87727465A>C , CM000672.2:g.87727465A>C | GRCh38 |
| NC_000010.10:g.89487222A>C , CM000672.1:g.89487222A>C | GRCh37 |
| NC_000010.9:g.89477202A>C | NCBI36 |
| NG_012150.1:g.72747A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000456849.2:c.1062A>C MANE Select | ENSP00000406157.1:p.Thr354= | |
| ENST00000361175.8:c.1047A>C | ENSP00000354436.4:p.Thr349= | |
| ENST00000456849.1:c.1062A>C | ENSP00000406157.1:p.Thr354= | |
| NM_001015880.1:c.1062A>C | NP_001015880.1:p.Thr354= | |
| NM_004670.3:c.1047A>C | NP_004661.2:p.Thr349= | |
| NM_001015880.2:c.1062A>C MANE Select | NP_001015880.1:p.Thr354= | |
| NM_004670.4:c.1047A>C | NP_004661.2:p.Thr349= |