HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21196778_21196779insCGTGTAG , CM000674.2:g.21196778_21196779insCGTGTAG | GRCh38 |
NC_000012.11:g.21349712_21349713insCGTGTAG , CM000674.1:g.21349712_21349713insCGTGTAG | GRCh37 |
NC_000012.10:g.21240979_21240980insCGTGTAG | NCBI36 |
NG_011745.1:g.70585_70586insCGTGTAG , LRG_1022:g.70585_70586insCGTGTAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.728-168_728-167insCGTGTAG MANE Select | ENSP00000256958.2:n.728-168_728-167insCGTGTAG | |
ENST00000256958.2:c.728-168_728-167insCGTGTAG | ENSP00000256958.2:n.728-168_728-167insCGTGTAG | |
NM_006446.4:c.728-168_728-167insCGTGTAG , LRG_1022t1:c.728-168_728-167insCGTGTAG | NP_006437.3:n.728-168_728-167insCGTGTAG | |
NM_006446.5:c.728-168_728-167insCGTGTAG MANE Select | NP_006437.3:n.728-168_728-167insCGTGTAG |