HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55156999T= , CM000681.2:g.55156999T= | GRCh38 |
NC_000019.9:g.55668367T= , CM000681.1:g.55668367T= | GRCh37 |
NC_000019.8:g.60360179T= | NCBI36 |
NG_007866.2:g.5734A= , LRG_432:g.5734A= | |
NG_032759.1:g.14724A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.108+51A= MANE Select | ENSP00000341838.5:n.108+51A= | |
ENST00000665070.1:c.108+51A= | ENSP00000499482.1:n.108+51A= | |
ENST00000344887.9:c.108+51A= | ENSP00000341838.5:n.108+51A= | |
ENST00000586446.1:n.301A= | ||
ENST00000586669.5:n.116+51A= | ||
ENST00000587176.5:n.292+51A= | ||
ENST00000587871.1:c.727+51A= | ||
ENST00000590463.1:n.280+51A= | ||
NM_000363.4:c.108+51A= , LRG_432t1:c.108+51A= | NP_000354.4:n.108+51A= | |
NM_000363.5:c.108+51A= MANE Select | NP_000354.4:n.108+51A= |