Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.37713392C>T , CM000684.2:g.37713392C>T | GRCh38 |
| NC_000022.10:g.38109399C>T , CM000684.1:g.38109399C>T | GRCh37 |
| NC_000022.9:g.36439345C>T | NCBI36 |
| NG_012857.1:g.21405C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644935.1:c.437C>T MANE Select | ENSP00000496394.1:p.Thr146Ile | |
| ENST00000344404.10:c.255-2371C>T | ENSP00000340312.6:n.255-2371C>T | |
| ENST00000406386.7:c.437C>T | ENSP00000384312.3:p.Thr146Ile | |
| ENST00000455236.4:c.1394C>T | ENSP00000477208.1:n.1394C>T | |
| ENST00000492485.5:n.391-2371C>T | ||
| NM_001039141.2:c.437C>T | NP_001034230.1:p.Thr146Ile | |
| NM_001039141.3:c.437C>T MANE Select | NP_001034230.1:p.Thr146Ile |