HGVS | Genome Assembly |
---|---|
NC_000022.11:g.42130839dup , CM000684.2:g.42130839dup | GRCh38 |
NC_000022.10:g.42526841dup , CM000684.1:g.42526841dup | GRCh37 |
NC_000022.9:g.40856785dup | NCBI36 |
NG_008376.3:g.4157dup | |
NG_008376.4:g.4976dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000359033.4:c.-44dup | ENSP00000351927.4:n.-44dup | |
ENST00000360608.9:c.-44dup | ENSP00000353820.5:n.-44dup | |
ENST00000389970.7:c.-110dup | ENSP00000374620.4:n.-110dup | |
NM_000106.5:c.-44dup | NP_000097.3:n.-44dup | |
NM_001025161.2:c.-44dup | NP_001020332.2:n.-44dup | |
XM_011529966.1:c.-44dup | XP_011528268.1:n.-44dup | |
XM_011529967.1:c.-44dup | XP_011528269.1:n.-44dup | |
XM_011529968.1:c.-44dup | XP_011528270.1:n.-44dup | |
XM_011529969.1:c.37+462dup | XP_011528271.1:n.37+462dup | |
XM_011529970.1:c.-44dup | XP_011528272.1:n.-44dup | |
XM_011529971.1:c.37+462dup | XP_011528273.1:n.37+462dup | |
XM_011529972.1:c.-44dup | XP_011528274.1:n.-44dup | |
XR_430455.2:n.328+151dup | ||
XR_002958749.1:n.275+151dup |