HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320371A= , CM000667.2:g.159320371A= | GRCh38 |
NC_000005.9:g.158747379A= , CM000667.1:g.158747379A= | GRCh37 |
NC_000005.8:g.158679957A= | NCBI36 |
NG_009618.1:g.15103T= , LRG_71:g.15103T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.2T= | ENSP00000512849.1:p.Met1= | |
ENST00000696751.1:c.*127T= | ENSP00000512850.1:n.*127T= | |
ENST00000231228.3:c.632T= MANE Select | ENSP00000231228.2:p.Met211= | |
ENST00000231228.2:c.632T= | ENSP00000231228.2:p.Met211= | |
NM_002187.2:c.632T= , LRG_71t1:c.632T= | NP_002178.2:p.Met211= | |
NM_002187.3:c.632T= MANE Select | NP_002178.2:p.Met211= |