HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990472_45990473insAGCGT , CM000683.2:g.45990472_45990473insAGCGT | GRCh38 |
NC_000021.8:g.47410386_47410387insAGCGT , CM000683.1:g.47410386_47410387insAGCGT | GRCh37 |
NC_000021.7:g.46234814_46234815insAGCGT | NCBI36 |
NG_008674.1:g.13724_13725insAGCGT , LRG_475:g.13724_13725insAGCGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+50_1002+51insAGCGT MANE Select | ENSP00000355180.3:n.1002+50_1002+51insAGCGT | |
ENST00000361866.7:c.1002+50_1002+51insAGCGT | ENSP00000355180.3:n.1002+50_1002+51insAGCGT | |
ENST00000612273.1:c.1002+50_1002+51insAGCGT | ENSP00000483630.1:n.1002+50_1002+51insAGCGT | |
NM_001848.2:c.1002+50_1002+51insAGCGT , LRG_475t1:c.1002+50_1002+51insAGCGT | NP_001839.2:n.1002+50_1002+51insAGCGT | |
NM_001848.3:c.1002+50_1002+51insAGCGT MANE Select | NP_001839.2:n.1002+50_1002+51insAGCGT |