HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315910_159315911del , CM000667.2:g.159315910_159315911del | GRCh38 |
NC_000005.9:g.158742918_158742919del , CM000667.1:g.158742918_158742919del | GRCh37 |
NC_000005.8:g.158675496_158675497del | NCBI36 |
NG_009618.1:g.19563_19564del , LRG_71:g.19563_19564del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.*190_*191del | ENSP00000512849.1:n.*190_*191del | |
ENST00000696751.1:c.*672_*673del | ENSP00000512850.1:n.*672_*673del | |
ENST00000231228.3:c.*190_*191del MANE Select | ENSP00000231228.2:n.*190_*191del | |
ENST00000231228.2:c.*190_*191del | ENSP00000231228.2:n.*190_*191del | |
NM_002187.2:c.*190_*191del , LRG_71t1:c.*190_*191del | NP_002178.2:n.*190_*191del | |
NM_002187.3:c.*190_*191del MANE Select | NP_002178.2:n.*190_*191del |