HGVS | Genome Assembly |
---|---|
NC_000005.10:g.96429045A= , CM000667.2:g.96429045A= | GRCh38 |
NC_000005.9:g.95764749A= , CM000667.1:g.95764749A= | GRCh37 |
NC_000005.8:g.95790505A= | NCBI36 |
NG_021161.1:g.9237T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311106.8:c.285+168T= MANE Select | ENSP00000308024.2:n.285+168T= | |
ENST00000311106.7:c.285+168T= | ENSP00000308024.2:n.285+168T= | |
ENST00000508626.5:c.144+168T= | ENSP00000421600.1:n.144+168T= | |
ENST00000509190.1:c.285+168T= | ENSP00000427294.1:n.285+168T= | |
NM_000439.4:c.285+168T= | NP_000430.3:n.285+168T= | |
NM_001177875.1:c.144+168T= | NP_001171346.1:n.144+168T= | |
NR_130776.1:n.354+49393A= | ||
NM_000439.5:c.285+168T= MANE Select | NP_000430.3:n.285+168T= | |
NM_001177875.2:c.144+168T= | NP_001171346.1:n.144+168T= |