HGVS | Genome Assembly |
---|---|
NC_000012.12:g.5046014C>T , CM000674.2:g.5046014C>T | GRCh38 |
NC_000012.11:g.5155180C>T , CM000674.1:g.5155180C>T | GRCh37 |
NC_000012.10:g.5025441C>T | NCBI36 |
NG_012198.1:g.7096C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252321.5:c.*25C>T MANE Select | ENSP00000252321.3:n.*25C>T | |
ENST00000252321.4:c.*25C>T | ENSP00000252321.3:n.*25C>T | |
NM_002234.3:c.*25C>T | NP_002225.2:n.*25C>T | |
NM_002234.4:c.*25C>T MANE Select | NP_002225.2:n.*25C>T |