HGVS | Genome Assembly |
---|---|
NC_000017.11:g.39665673_39665674del , CM000679.2:g.39665673_39665674del | GRCh38 |
NC_000017.10:g.37821926_37821927del , CM000679.1:g.37821926_37821927del | GRCh37 |
NC_000017.9:g.35075452_35075453del | NCBI36 |
NG_008892.1:g.5328_5329del , LRG_210:g.5328_5329del | |
NG_042278.1:g.2693_2694del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309889.3:c.111-43_111-42del MANE Select | ENSP00000312624.2:n.111-43_111-42del | |
ENST00000309889.2:c.111-43_111-42del | ENSP00000312624.2:n.111-43_111-42del | |
ENST00000578283.1:c.111-43_111-42del | ENSP00000462787.1:n.111-43_111-42del | |
NM_003673.3:c.111-43_111-42del , LRG_210t1:c.111-43_111-42del | NP_003664.1:n.111-43_111-42del | |
NM_003673.4:c.111-43_111-42del MANE Select | NP_003664.1:n.111-43_111-42del |