HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38148693_38148694delinsGC , CM000670.2:g.38148693_38148694delinsGC | GRCh38 |
NC_000008.10:g.38006211_38006212delinsGC , CM000670.1:g.38006211_38006212delinsGC | GRCh37 |
NC_000008.9:g.38125368_38125369delinsGC | NCBI36 |
NG_011827.1:g.7389_7390delinsGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000276449.9:c.125_126delinsGC MANE Select | ENSP00000276449.3:p.Gly42= | |
ENST00000276449.8:c.125_126delinsGC | ENSP00000276449.3:p.Gly42= | |
ENST00000520114.1:n.299_300delinsGC | ||
ENST00000521236.1:c.-154_-153delinsGC | ENSP00000430030.1:n.-154_-153delinsGC | |
ENST00000522050.1:c.61_62delinsGC | ||
NM_000349.2:c.125_126delinsGC | NP_000340.2:p.Gly42= | |
XM_006716392.1:c.125_126delinsGC | XP_006716455.1:p.Gly42= | |
NM_000349.3:c.125_126delinsGC MANE Select | NP_000340.2:p.Gly42= |