HGVS | Genome Assembly |
---|---|
NC_000006.12:g.143485279dup , CM000668.2:g.143485279dup | GRCh38 |
NC_000006.11:g.143806416dup , CM000668.1:g.143806416dup | GRCh37 |
NC_000006.10:g.143848109dup | NCBI36 |
NG_008459.1:g.39499dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367591.5:c.1038+31dup MANE Select | ENSP00000356563.4:n.1038+31dup | |
ENST00000367591.4:c.1038+31dup | ENSP00000356563.4:n.1038+31dup | |
ENST00000585848.1:n.177+31dup | ||
NM_003630.2:c.1038+31dup | NP_003621.1:n.1038+31dup | |
NM_003630.3:c.1038+31dup MANE Select | NP_003621.1:n.1038+31dup |