HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35847849_35847850delinsAT , CM000681.2:g.35847849_35847850delinsAT | GRCh38 |
NC_000019.9:g.36338751_36338752delinsAT , CM000681.1:g.36338751_36338752delinsAT | GRCh37 |
NC_000019.8:g.41030591_41030592delinsAT | NCBI36 |
NG_013356.2:g.26438_26439delinsAT , LRG_693:g.26438_26439delinsAT | |
NG_051206.1:g.1215_1216delinsAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378910.10:c.1440+191_1440+192delinsAT MANE Select | ENSP00000368190.4:n.1440+191_1440+192delinsAT | |
ENST00000353632.6:c.1440+191_1440+192delinsAT | ENSP00000343634.5:n.1440+191_1440+192delinsAT | |
ENST00000378910.9:c.1440+191_1440+192delinsAT | ENSP00000368190.4:n.1440+191_1440+192delinsAT | |
NM_004646.3:c.1440+191_1440+192delinsAT , LRG_693t1:c.1440+191_1440+192delinsAT | NP_004637.1:n.1440+191_1440+192delinsAT | |
NM_004646.4:c.1440+191_1440+192delinsAT MANE Select | NP_004637.1:n.1440+191_1440+192delinsAT |