HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46011519dup , CM000682.2:g.46011519dup | GRCh38 |
NC_000020.10:g.44640158dup , CM000682.1:g.44640158dup | GRCh37 |
NC_000020.9:g.44073565dup | NCBI36 |
NG_011468.1:g.7612dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372330.3:c.824-55dup MANE Select | ENSP00000361405.3:n.824-55dup | |
NM_004994.2:c.824-55dup | NP_004985.2:n.824-55dup | |
NM_004994.3:c.824-55dup MANE Select | NP_004985.2:n.824-55dup |