HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315979T= , CM000667.2:g.159315979T= | GRCh38 |
NC_000005.9:g.158742987T= , CM000667.1:g.158742987T= | GRCh37 |
NC_000005.8:g.158675565T= | NCBI36 |
NG_009618.1:g.19495A= , LRG_71:g.19495A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.*122A= | ENSP00000512849.1:n.*122A= | |
ENST00000696751.1:c.*604A= | ENSP00000512850.1:n.*604A= | |
ENST00000231228.3:c.*122A= MANE Select | ENSP00000231228.2:n.*122A= | |
ENST00000231228.2:c.*122A= | ENSP00000231228.2:n.*122A= | |
NM_002187.2:c.*122A= , LRG_71t1:c.*122A= | NP_002178.2:n.*122A= | |
NM_002187.3:c.*122A= MANE Select | NP_002178.2:n.*122A= |