HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6072291dup , CM000674.2:g.6072291dup | GRCh38 |
NC_000012.11:g.6181457dup , CM000674.1:g.6181457dup | GRCh37 |
NC_000012.10:g.6051718dup | NCBI36 |
NG_009072.1:g.57384dup | |
NG_009072.2:g.57384dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261405.10:c.1109+44dup MANE Select | ENSP00000261405.5:n.1109+44dup | |
ENST00000261405.9:c.1109+44dup | ENSP00000261405.5:n.1109+44dup | |
ENST00000538635.5:n.420+38228dup | ||
NM_000552.3:c.1109+44dup | NP_000543.2:n.1109+44dup | |
NM_000552.4:c.1109+44dup | NP_000543.2:n.1109+44dup | |
NM_000552.5:c.1109+44dup MANE Select | NP_000543.3:n.1109+44dup |