HGVS | Genome Assembly |
---|---|
NC_000020.11:g.6770056_6770057insT , CM000682.2:g.6770056_6770057insT | GRCh38 |
NC_000020.10:g.6750703_6750704insT , CM000682.1:g.6750703_6750704insT | GRCh37 |
NC_000020.9:g.6698703_6698704insT | NCBI36 |
NG_023233.1:g.6959_6960insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378827.5:c.-7-64_-7-63insT MANE Select | ENSP00000368104.3:n.-7-64_-7-63insT | |
ENST00000378827.4:c.-7-64_-7-63insT | ENSP00000368104.3:n.-7-64_-7-63insT | |
NM_001200.2:c.-7-64_-7-63insT | NP_001191.1:n.-7-64_-7-63insT | |
XM_011529323.1:c.-123+1181_-123+1182insT | XP_011527625.1:n.-123+1181_-123+1182insT | |
NM_001200.3:c.-7-64_-7-63insT | NP_001191.1:n.-7-64_-7-63insT | |
NM_001200.4:c.-7-64_-7-63insT MANE Select | NP_001191.1:n.-7-64_-7-63insT |