HGVS | Genome Assembly |
---|---|
NC_000002.12:g.216205574_216205575delinsGA , CM000664.2:g.216205574_216205575delinsGA | GRCh38 |
NC_000002.11:g.217070297_217070298delinsGA , CM000664.1:g.217070297_217070298delinsGA | GRCh37 |
NC_000002.10:g.216778542_216778543delinsGA | NCBI36 |
NG_029780.1:g.101278_101279delinsGA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000392132.7:c.*372_*373delinsGA MANE Select | ENSP00000375977.2:n.*372_*373delinsGA | |
ENST00000392132.6:c.*372_*373delinsGA | ENSP00000375977.2:n.*372_*373delinsGA | |
ENST00000392133.7:c.*372_*373delinsGA | ENSP00000375978.3:n.*372_*373delinsGA | |
NM_021141.3:c.*372_*373delinsGA | NP_066964.1:n.*372_*373delinsGA | |
NM_021141.4:c.*372_*373delinsGA MANE Select | NP_066964.1:n.*372_*373delinsGA |