HGVS | Genome Assembly |
---|---|
NC_000013.11:g.33055639dup , CM000675.2:g.33055639dup | GRCh38 |
NC_000013.10:g.33629776dup , CM000675.1:g.33629776dup | GRCh37 |
NC_000013.9:g.32527776dup | NCBI36 |
NG_011485.1:g.44206dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380099.4:c.1599+324dup MANE Select | ENSP00000369442.3:n.1599+324dup | |
ENST00000380099.3:c.1599+324dup | ENSP00000369442.3:n.1599+324dup | |
ENST00000487852.1:n.1657+274dup | ||
NM_004795.3:c.1599+324dup | NP_004786.2:n.1599+324dup | |
XM_006719895.1:c.678+324dup | XP_006719958.1:n.678+324dup | |
XM_006719895.2:c.678+324dup | XP_006719958.1:n.678+324dup | |
NM_004795.4:c.1599+324dup MANE Select | NP_004786.2:n.1599+324dup |