HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35845967_35845968delinsCT , CM000681.2:g.35845967_35845968delinsCT | GRCh38 |
NC_000019.9:g.36336869_36336870delinsCT , CM000681.1:g.36336869_36336870delinsCT | GRCh37 |
NC_000019.8:g.41028709_41028710delinsCT | NCBI36 |
NG_013356.2:g.28320_28321delinsAG , LRG_693:g.28320_28321delinsAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378910.10:c.1627+40_1627+41delinsAG MANE Select | ENSP00000368190.4:n.1627+40_1627+41delinsAG | |
ENST00000353632.6:c.1627+40_1627+41delinsAG | ENSP00000343634.5:n.1627+40_1627+41delinsAG | |
ENST00000378910.9:c.1627+40_1627+41delinsAG | ENSP00000368190.4:n.1627+40_1627+41delinsAG | |
NM_004646.3:c.1627+40_1627+41delinsAG , LRG_693t1:c.1627+40_1627+41delinsAG | NP_004637.1:n.1627+40_1627+41delinsAG | |
NM_004646.4:c.1627+40_1627+41delinsAG MANE Select | NP_004637.1:n.1627+40_1627+41delinsAG |