Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8003529C= , CM000679.2:g.8003529C= | GRCh38 |
| NC_000017.10:g.7906847C= , CM000679.1:g.7906847C= | GRCh37 |
| NC_000017.9:g.7847572C= | NCBI36 |
| NG_009092.1:g.5860C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254854.5:c.482C= MANE Select | ENSP00000254854.4:p.Thr161= | |
| ENST00000254854.4:c.482C= | ENSP00000254854.4:p.Thr161= | |
| NM_000180.3:c.482C= | NP_000171.1:p.Thr161= | |
| XM_011523816.1:c.482C= | XP_011522118.1:p.Thr161= | |
| NM_000180.4:c.482C= MANE Select | NP_000171.1:p.Thr161= |