HGVS | Genome Assembly |
---|---|
NC_000011.10:g.62909247_62909248delinsTC , CM000673.2:g.62909247_62909248delinsTC | GRCh38 |
NC_000011.9:g.62676719_62676720delinsTC , CM000673.1:g.62676719_62676720delinsTC | GRCh37 |
NC_000011.8:g.62433295_62433296delinsTC | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000306960.4:c.*470_*471delinsGA MANE Select | ENSP00000306490.3:n.*470_*471delinsGA | |
ENST00000306960.3:c.*470_*471delinsGA | ENSP00000306490.3:n.*470_*471delinsGA | |
NM_000738.2:c.*470_*471delinsGA | NP_000729.2:n.*470_*471delinsGA | |
XM_011544742.1:c.*470_*471delinsGA | XP_011543044.1:n.*470_*471delinsGA | |
XM_011544742.2:c.*470_*471delinsGA | XP_011543044.1:n.*470_*471delinsGA | |
NM_000738.3:c.*470_*471delinsGA MANE Select | NP_000729.2:n.*470_*471delinsGA |