HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55157628G= , CM000681.2:g.55157628G= | GRCh38 |
NC_000019.9:g.55668996G= , CM000681.1:g.55668996G= | GRCh37 |
NC_000019.8:g.60360808G= | NCBI36 |
NG_007866.2:g.5105C= , LRG_432:g.5105C= | |
NG_032759.1:g.14095C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.-39C= MANE Select | ENSP00000341838.5:n.-39C= | |
ENST00000665070.1:c.-39C= | ENSP00000499482.1:n.-39C= | |
ENST00000344887.9:c.-39C= | ENSP00000341838.5:n.-39C= | |
ENST00000586446.1:n.105C= | ||
ENST00000587176.5:n.146C= | ||
ENST00000587871.1:c.582C= | ||
ENST00000590463.1:n.89C= | ||
NM_000363.4:c.-39C= , LRG_432t1:c.-39C= | NP_000354.4:n.-39C= | |
NM_000363.5:c.-39C= MANE Select | NP_000354.4:n.-39C= |