HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55157648T= , CM000681.2:g.55157648T= | GRCh38 |
NC_000019.9:g.55669016T= , CM000681.1:g.55669016T= | GRCh37 |
NC_000019.8:g.60360828T= | NCBI36 |
NG_007866.2:g.5085A= , LRG_432:g.5085A= | |
NG_032759.1:g.14075A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.-59A= MANE Select | ENSP00000341838.5:n.-59A= | |
ENST00000665070.1:c.-59A= | ENSP00000499482.1:n.-59A= | |
ENST00000344887.9:c.-59A= | ENSP00000341838.5:n.-59A= | |
ENST00000586446.1:n.85A= | ||
ENST00000587176.5:n.126A= | ||
ENST00000587871.1:c.562A= | ||
ENST00000590463.1:n.69A= | ||
NM_000363.4:c.-59A= , LRG_432t1:c.-59A= | NP_000354.4:n.-59A= | |
NM_000363.5:c.-59A= MANE Select | NP_000354.4:n.-59A= |