HGVS | Genome Assembly |
---|---|
NC_000005.10:g.44305206_44305208dup , CM000667.2:g.44305206_44305208dup | GRCh38 |
NC_000005.9:g.44305308_44305310dup , CM000667.1:g.44305308_44305310dup | GRCh37 |
NC_000005.8:g.44341065_44341067dup | NCBI36 |
NG_011446.1:g.88476_88478dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264664.5:c.430-15_430-13dup MANE Select | ENSP00000264664.4:n.430-15_430-13dup | |
ENST00000264664.4:c.430-15_430-13dup | ENSP00000264664.4:n.430-15_430-13dup | |
NM_004465.1:c.430-15_430-13dup | NP_004456.1:n.430-15_430-13dup | |
XM_005248264.2:c.430-15_430-13dup | XP_005248321.1:n.430-15_430-13dup | |
XM_005248264.4:c.430-15_430-13dup | XP_005248321.1:n.430-15_430-13dup | |
NM_004465.2:c.430-15_430-13dup MANE Select | NP_004456.1:n.430-15_430-13dup |