HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22624000_22624002dup , CM000673.2:g.22624000_22624002dup | GRCh38 |
NC_000011.9:g.22645546_22645548dup , CM000673.1:g.22645546_22645548dup | GRCh37 |
NC_000011.8:g.22602122_22602124dup | NCBI36 |
NG_007425.1:g.6849_6851dup , LRG_527:g.6849_6851dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000327470.6:c.*693_*695dup MANE Select | ENSP00000330875.3:n.*693_*695dup | |
ENST00000327470.4:c.*693_*695dup | ENSP00000330875.3:n.*693_*695dup | |
NM_022725.3:c.*693_*695dup , LRG_527t1:c.*693_*695dup | NP_073562.1:n.*693_*695dup | |
NM_022725.4:c.*693_*695dup MANE Select | NP_073562.1:n.*693_*695dup |