HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47003949_47003952del , CM000681.2:g.47003949_47003952del | GRCh38 |
NC_000019.9:g.47507206_47507209del , CM000681.1:g.47507206_47507209del | GRCh37 |
NC_000019.8:g.52199046_52199049del | NCBI36 |
NG_047014.1:g.90383_90386del | |
NG_047014.2:g.147953_147956del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000404338.8:c.7761_7764del | ENSP00000385720.2:n.7761_7764del | |
ENST00000672722.1:c.*3261_*3264del MANE Select | ENSP00000500409.1:n.*3261_*3264del | |
ENST00000404338.7:c.7761_7764del | ENSP00000385720.2:n.7761_7764del | |
ENST00000614079.1:c.7338_7341del | ENSP00000483730.1:n.7338_7341del | |
NM_004491.4:c.7761_7764del | NP_004482.4:n.7761_7764del | |
NM_004491.5:c.*3261_*3264del MANE Select | NP_004482.4:n.*3261_*3264del |