HGVS | Genome Assembly |
---|---|
NC_000001.11:g.46399238_46399246dup , CM000663.2:g.46399238_46399246dup | GRCh38 |
NC_000001.10:g.46864910_46864918dup , CM000663.1:g.46864910_46864918dup | GRCh37 |
NC_000001.9:g.46637497_46637505dup | NCBI36 |
NG_012195.1:g.9972_9980dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243167.9:c.196-2853_196-2845dup MANE Select | ENSP00000243167.8:n.196-2853_196-2845dup | |
ENST00000243167.8:c.196-2853_196-2845dup | ENSP00000243167.8:n.196-2853_196-2845dup | |
ENST00000468718.5:n.216-2853_216-2845dup | ||
ENST00000493735.5:n.174-2853_174-2845dup | ||
NM_001441.2:c.196-2853_196-2845dup | NP_001432.2:n.196-2853_196-2845dup | |
NM_001441.3:c.196-2853_196-2845dup MANE Select | NP_001432.2:n.196-2853_196-2845dup |