HGVS | Genome Assembly |
---|---|
NC_000001.11:g.159886609T>G , CM000663.2:g.159886609T>G | GRCh38 |
NC_000001.10:g.159856399T>G , CM000663.1:g.159856399T>G | GRCh37 |
NC_000001.9:g.158123023T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368099.9:c.669A>C MANE Select | ENSP00000357079.4:p.Thr223= | |
ENST00000368099.8:c.669A>C | ENSP00000357079.4:p.Thr223= | |
ENST00000426543.6:c.414A>C | ENSP00000403044.2:p.Thr138= | |
ENST00000476696.5:c.669A>C | ENSP00000483972.1:p.Thr223= | |
ENST00000479940.2:c.414A>C | ENSP00000478944.1:p.Thr138= | |
NM_012337.2:c.669A>C | NP_036469.2:p.Thr223= | |
NM_012337.3:c.669A>C MANE Select | NP_036469.2:p.Thr223= |