HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229431620T>G , CM000663.2:g.229431620T>G | GRCh38 |
NC_000001.10:g.229567367T>G , CM000663.1:g.229567367T>G | GRCh37 |
NC_000001.9:g.227633990T>G | NCBI36 |
NG_006672.1:g.7477A>C , LRG_429:g.7477A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366683.4:c.991-56A>C | ENSP00000355644.4:n.991-56A>C | |
ENST00000684723.1:c.878A>C | ENSP00000508084.1:p.Lys293Thr | |
ENST00000366683.3:c.644A>C | ENSP00000355644.3:p.Lys215Thr | |
ENST00000366684.7:c.1013A>C MANE Select | ENSP00000355645.3:p.Lys338Thr | |
NM_001100.3:c.1013A>C , LRG_429t1:c.1013A>C | NP_001091.1:p.Lys338Thr | |
NM_001100.4:c.1013A>C MANE Select | NP_001091.1:p.Lys338Thr |