HGVS | Genome Assembly |
---|---|
NC_000018.10:g.13884460_13884463dup , CM000680.2:g.13884460_13884463dup | GRCh38 |
NC_000018.9:g.13884459_13884462dup , CM000680.1:g.13884459_13884462dup | GRCh37 |
NC_000018.8:g.13874459_13874462dup | NCBI36 |
NG_011819.1:g.36074_36077dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327606.4:c.*162_*165dup MANE Select | ENSP00000333821.2:n.*162_*165dup | |
ENST00000327606.3:c.*162_*165dup | ENSP00000333821.2:n.*162_*165dup | |
NM_000529.2:c.*162_*165dup MANE Select | NP_000520.1:n.*162_*165dup | |
NM_001291911.1:c.*162_*165dup | NP_001278840.1:n.*162_*165dup | |
XM_017025781.1:c.*162_*165dup | XP_016881270.1:n.*162_*165dup |