HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35845964_35845965insG , CM000681.2:g.35845964_35845965insG | GRCh38 |
NC_000019.9:g.36336866_36336867insG , CM000681.1:g.36336866_36336867insG | GRCh37 |
NC_000019.8:g.41028706_41028707insG | NCBI36 |
NG_013356.2:g.28323_28324insC , LRG_693:g.28323_28324insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378910.10:c.1627+43_1627+44insC MANE Select | ENSP00000368190.4:n.1627+43_1627+44insC | |
ENST00000353632.6:c.1627+43_1627+44insC | ENSP00000343634.5:n.1627+43_1627+44insC | |
ENST00000378910.9:c.1627+43_1627+44insC | ENSP00000368190.4:n.1627+43_1627+44insC | |
NM_004646.3:c.1627+43_1627+44insC , LRG_693t1:c.1627+43_1627+44insC | NP_004637.1:n.1627+43_1627+44insC | |
NM_004646.4:c.1627+43_1627+44insC MANE Select | NP_004637.1:n.1627+43_1627+44insC |