Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35651285C>T , CM000681.2:g.35651285C>T | GRCh38 |
| NC_000019.9:g.36142187C>T , CM000681.1:g.36142187C>T | GRCh37 |
| NC_000019.8:g.40834027C>T | NCBI36 |
| NG_012193.1:g.8033C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000592141.6:c.42C>T | ENSP00000466818.2:p.Thr14= | |
| ENST00000649813.2:c.42C>T MANE Select | ENSP00000497926.1:p.Thr14= | |
| ENST00000652250.1:c.42C>T | ENSP00000498883.1:p.Thr14= | |
| ENST00000246554.7:c.42C>T | ENSP00000246554.2:p.Thr14= | |
| ENST00000392201.1:c.42C>T | ENSP00000376037.2:p.Thr14= | |
| ENST00000590618.1:c.41C>T | ||
| ENST00000592141.5:c.42C>T | ENSP00000466818.2:p.Thr14= | |
| NM_001863.4:c.42C>T | NP_001854.1:p.Thr14= | |
| NM_001863.5:c.42C>T MANE Select | NP_001854.1:p.Thr14= |