HGVS | Genome Assembly |
---|---|
NC_000008.11:g.24956578dup , CM000670.2:g.24956578dup | GRCh38 |
NC_000008.10:g.24814092dup , CM000670.1:g.24814092dup | GRCh37 |
NC_000008.9:g.24870009dup | NCBI36 |
NG_008492.1:g.5043dup , LRG_259:g.5043dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000610854.2:c.-60dup MANE Select | ENSP00000482169.2:n.-60dup | |
ENST00000610854.1:c.-60dup | ENSP00000482169.1:n.-60dup | |
ENST00000615973.1:n.147dup | ||
ENST00000619417.1:c.-60dup | ENSP00000483690.1:n.-60dup | |
NM_006158.4:c.-60dup , LRG_259t1:c.-60dup | NP_006149.2:n.-60dup | |
NM_006158.5:c.-60dup MANE Select | NP_006149.2:n.-60dup |