HGVS | Genome Assembly |
---|---|
NC_000017.11:g.34255429_34255431dup , CM000679.2:g.34255429_34255431dup | GRCh38 |
NC_000017.10:g.32582448_32582450dup , CM000679.1:g.32582448_32582450dup | GRCh37 |
NC_000017.9:g.29606561_29606563dup | NCBI36 |
NG_012123.1:g.5153_5155dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000580907.6:c.76+4_76+6dup | ENSP00000462156.1:n.76+4_76+6dup | |
ENST00000624362.2:n.145_147dup | ||
ENST00000225831.4:c.76+4_76+6dup MANE Select | ENSP00000225831.4:n.76+4_76+6dup | |
ENST00000580907.5:c.76+4_76+6dup | ENSP00000462156.1:n.76+4_76+6dup | |
ENST00000624362.1:n.212_214dup | ||
NM_002982.3:c.76+4_76+6dup | NP_002973.1:n.76+4_76+6dup | |
NM_002982.4:c.76+4_76+6dup MANE Select | NP_002973.1:n.76+4_76+6dup |