HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315945C>A , CM000667.2:g.159315945C>A | GRCh38 |
NC_000005.9:g.158742953C>A , CM000667.1:g.158742953C>A | GRCh37 |
NC_000005.8:g.158675531C>A | NCBI36 |
NG_009618.1:g.19529G>T , LRG_71:g.19529G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.*156G>T | ENSP00000512849.1:n.*156G>T | |
ENST00000696751.1:c.*638G>T | ENSP00000512850.1:n.*638G>T | |
ENST00000231228.3:c.*156G>T MANE Select | ENSP00000231228.2:n.*156G>T | |
ENST00000231228.2:c.*156G>T | ENSP00000231228.2:n.*156G>T | |
NM_002187.2:c.*156G>T , LRG_71t1:c.*156G>T | NP_002178.2:n.*156G>T | |
NM_002187.3:c.*156G>T MANE Select | NP_002178.2:n.*156G>T |