HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443752_32443753del , CM000668.2:g.32443752_32443753del | GRCh38 |
NC_000006.11:g.32411529_32411530del , CM000668.1:g.32411529_32411530del | GRCh37 |
NC_000006.10:g.32519507_32519508del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000395388.7:c.611-4_611-3del MANE Select | ENSP00000378786.2:n.611-4_611-3del | |
ENST00000374982.5:c.536-4_536-3del | ENSP00000364121.5:n.536-4_536-3del | |
ENST00000395388.6:c.611-4_611-3del | ENSP00000378786.2:n.611-4_611-3del | |
NM_019111.4:c.611-4_611-3del | NP_061984.2:n.611-4_611-3del | |
NM_019111.5:c.611-4_611-3del MANE Select | NP_061984.2:n.611-4_611-3del |