HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135186_26135187delinsAC , CM000664.2:g.26135186_26135187delinsAC | GRCh38 |
NC_000002.11:g.26358055_26358056delinsAC , CM000664.1:g.26358055_26358056delinsAC | GRCh37 |
NC_000002.10:g.26211559_26211560delinsAC | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*165_*166delinsAC MANE Select | ENSP00000264710.4:n.*165_*166delinsAC | |
ENST00000264710.4:c.*165_*166delinsAC | ENSP00000264710.4:n.*165_*166delinsAC | |
ENST00000495146.5:n.1131_1132delinsAC | ||
NM_016131.4:c.*165_*166delinsAC | NP_057215.3:n.*165_*166delinsAC | |
XM_024452565.1:c.*165_*166delinsAC | XP_024308333.1:n.*165_*166delinsAC | |
NM_016131.5:c.*165_*166delinsAC MANE Select | NP_057215.3:n.*165_*166delinsAC |