HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315956C= , CM000667.2:g.159315956C= | GRCh38 |
NC_000005.9:g.158742964C= , CM000667.1:g.158742964C= | GRCh37 |
NC_000005.8:g.158675542C= | NCBI36 |
NG_009618.1:g.19518G= , LRG_71:g.19518G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.*145G= | ENSP00000512849.1:n.*145G= | |
ENST00000696751.1:c.*627G= | ENSP00000512850.1:n.*627G= | |
ENST00000231228.3:c.*145G= MANE Select | ENSP00000231228.2:n.*145G= | |
ENST00000231228.2:c.*145G= | ENSP00000231228.2:n.*145G= | |
NM_002187.2:c.*145G= , LRG_71t1:c.*145G= | NP_002178.2:n.*145G= | |
NM_002187.3:c.*145G= MANE Select | NP_002178.2:n.*145G= |