HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35848000del , CM000681.2:g.35848000del | GRCh38 |
NC_000019.9:g.36338902del , CM000681.1:g.36338902del | GRCh37 |
NC_000019.8:g.41030742del | NCBI36 |
NG_013356.2:g.26292del , LRG_693:g.26292del | |
NG_051206.1:g.1366del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378910.10:c.1440+45del MANE Select | ENSP00000368190.4:n.1440+45del | |
ENST00000353632.6:c.1440+45del | ENSP00000343634.5:n.1440+45del | |
ENST00000378910.9:c.1440+45del | ENSP00000368190.4:n.1440+45del | |
ENST00000592132.1:n.492del | ||
NM_004646.3:c.1440+45del , LRG_693t1:c.1440+45del | NP_004637.1:n.1440+45del | |
NM_004646.4:c.1440+45del MANE Select | NP_004637.1:n.1440+45del |