HGVS | Genome Assembly |
---|---|
NC_000008.11:g.38145151dup , CM000670.2:g.38145151dup | GRCh38 |
NC_000008.10:g.38002669dup , CM000670.1:g.38002669dup | GRCh37 |
NC_000008.9:g.38121826dup | NCBI36 |
NG_011827.1:g.10932dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000276449.9:c.744+71dup MANE Select | ENSP00000276449.3:n.744+71dup | |
ENST00000276449.8:c.744+71dup | ENSP00000276449.3:n.744+71dup | |
ENST00000520114.1:n.1949dup | ||
ENST00000522050.1:c.587-765dup | ||
NM_000349.2:c.744+71dup | NP_000340.2:n.744+71dup | |
XM_006716392.1:c.651-765dup | XP_006716455.1:n.651-765dup | |
NM_000349.3:c.744+71dup MANE Select | NP_000340.2:n.744+71dup |