HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38145868_38145869delinsGT , CM000670.2:g.38145868_38145869delinsGT | GRCh38 |
NC_000008.10:g.38003386_38003387delinsGT , CM000670.1:g.38003386_38003387delinsGT | GRCh37 |
NC_000008.9:g.38122543_38122544delinsGT | NCBI36 |
NG_011827.1:g.10214_10215delinsAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000276449.9:c.650+94_650+95delinsAC MANE Select | ENSP00000276449.3:n.650+94_650+95delinsAC | |
ENST00000276449.8:c.650+94_650+95delinsAC | ENSP00000276449.3:n.650+94_650+95delinsAC | |
ENST00000520114.1:n.1231_1232delinsAC | ||
ENST00000522050.1:c.586+94_586+95delinsAC | ||
NM_000349.2:c.650+94_650+95delinsAC | NP_000340.2:n.650+94_650+95delinsAC | |
XM_006716392.1:c.650+94_650+95delinsAC | XP_006716455.1:n.650+94_650+95delinsAC | |
NM_000349.3:c.650+94_650+95delinsAC MANE Select | NP_000340.2:n.650+94_650+95delinsAC |