HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55157641T= , CM000681.2:g.55157641T= | GRCh38 |
NC_000019.9:g.55669009T= , CM000681.1:g.55669009T= | GRCh37 |
NC_000019.8:g.60360821T= | NCBI36 |
NG_007866.2:g.5092A= , LRG_432:g.5092A= | |
NG_032759.1:g.14082A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.-52A= MANE Select | ENSP00000341838.5:n.-52A= | |
ENST00000665070.1:c.-52A= | ENSP00000499482.1:n.-52A= | |
ENST00000344887.9:c.-52A= | ENSP00000341838.5:n.-52A= | |
ENST00000586446.1:n.92A= | ||
ENST00000587176.5:n.133A= | ||
ENST00000587871.1:c.569A= | ||
ENST00000590463.1:n.76A= | ||
NM_000363.4:c.-52A= , LRG_432t1:c.-52A= | NP_000354.4:n.-52A= | |
NM_000363.5:c.-52A= MANE Select | NP_000354.4:n.-52A= |