Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7524980C>T , CM000681.2:g.7524980C>T | GRCh38 |
| NC_000019.9:g.7589866C>T , CM000681.1:g.7589866C>T | GRCh37 |
| NC_000019.8:g.7495866C>T | NCBI36 |
| NG_015806.1:g.7371C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.51C>T MANE Select | ENSP00000264079.5:p.Thr17= | |
| ENST00000264079.10:c.51C>T | ENSP00000264079.5:p.Thr17= | |
| ENST00000394321.9:n.131C>T | ||
| ENST00000596390.1:n.167C>T | ||
| ENST00000601003.1:c.51C>T | ENSP00000469074.1:p.Thr17= | |
| NM_020533.2:c.51C>T | NP_065394.1:p.Thr17= | |
| XR_936293.2:n.1G>A | ||
| XR_936294.2:n.1G>A | ||
| NM_020533.3:c.51C>T MANE Select | NP_065394.1:p.Thr17= |