HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38145560_38145562dup , CM000670.2:g.38145560_38145562dup | GRCh38 |
NC_000008.10:g.38003078_38003080dup , CM000670.1:g.38003078_38003080dup | GRCh37 |
NC_000008.9:g.38122235_38122237dup | NCBI36 |
NG_011827.1:g.10521_10523dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000276449.9:c.651-247_651-245dup MANE Select | ENSP00000276449.3:n.651-247_651-245dup | |
ENST00000276449.8:c.651-247_651-245dup | ENSP00000276449.3:n.651-247_651-245dup | |
ENST00000520114.1:n.1538_1540dup | ||
ENST00000522050.1:c.586+401_586+403dup | ||
NM_000349.2:c.651-247_651-245dup | NP_000340.2:n.651-247_651-245dup | |
XM_006716392.1:c.650+401_650+403dup | XP_006716455.1:n.650+401_650+403dup | |
NM_000349.3:c.651-247_651-245dup MANE Select | NP_000340.2:n.651-247_651-245dup |