HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55157624G= , CM000681.2:g.55157624G= | GRCh38 |
NC_000019.9:g.55668992G= , CM000681.1:g.55668992G= | GRCh37 |
NC_000019.8:g.60360804G= | NCBI36 |
NG_007866.2:g.5109C= , LRG_432:g.5109C= | |
NG_032759.1:g.14099C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.-35C= MANE Select | ENSP00000341838.5:n.-35C= | |
ENST00000665070.1:c.-35C= | ENSP00000499482.1:n.-35C= | |
ENST00000344887.9:c.-35C= | ENSP00000341838.5:n.-35C= | |
ENST00000586446.1:n.109C= | ||
ENST00000587176.5:n.150C= | ||
ENST00000587871.1:c.586C= | ||
ENST00000590463.1:n.93C= | ||
NM_000363.4:c.-35C= , LRG_432t1:c.-35C= | NP_000354.4:n.-35C= | |
NM_000363.5:c.-35C= MANE Select | NP_000354.4:n.-35C= |