HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23420322_23420323delinsAC , CM000676.2:g.23420322_23420323delinsAC | GRCh38 |
NC_000014.8:g.23889531_23889532delinsAC , CM000676.1:g.23889531_23889532delinsAC | GRCh37 |
NC_000014.7:g.22959371_22959372delinsAC | NCBI36 |
NG_007884.1:g.20339_20340delinsGT , LRG_384:g.20339_20340delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3337-89_3337-88delinsGT MANE Select | ENSP00000347507.3:n.3337-89_3337-88delinsGT | |
ENST00000355349.3:c.3337-89_3337-88delinsGT | ENSP00000347507.3:n.3337-89_3337-88delinsGT | |
NM_000257.3:c.3337-89_3337-88delinsGT | NP_000248.2:n.3337-89_3337-88delinsGT | |
XR_245686.3:n.3445-89_3445-88delinsGT | ||
XM_017021340.1:c.3337-89_3337-88delinsGT | XP_016876829.1:n.3337-89_3337-88delinsGT | |
NM_000257.4:c.3337-89_3337-88delinsGT MANE Select | NP_000248.2:n.3337-89_3337-88delinsGT |