HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41583728_41583729insTC , CM000679.2:g.41583728_41583729insTC | GRCh38 |
NC_000017.10:g.39739980_39739981insTC , CM000679.1:g.39739980_39739981insTC | GRCh37 |
NC_000017.9:g.36993506_36993507insTC | NCBI36 |
NG_008624.1:g.8167_8168insGA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000167586.7:c.927+31_927+32insGA MANE Select | ENSP00000167586.6:n.927+31_927+32insGA | |
ENST00000167586.6:c.927+31_927+32insGA | ENSP00000167586.6:n.927+31_927+32insGA | |
ENST00000476662.1:n.377+31_377+32insGA | ||
NM_000526.4:c.927+31_927+32insGA | NP_000517.2:n.927+31_927+32insGA | |
NM_000526.5:c.927+31_927+32insGA MANE Select | NP_000517.3:n.927+31_927+32insGA |