HGVS | Genome Assembly |
---|---|
NC_000002.12:g.188996079dup , CM000664.2:g.188996079dup | GRCh38 |
NC_000002.11:g.189860805dup , CM000664.1:g.189860805dup | GRCh37 |
NC_000002.10:g.189569050dup | NCBI36 |
NG_007404.1:g.26707dup , LRG_3:g.26707dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000450867.2:c.1510-46dup | ENSP00000415346.2:n.1510-46dup | |
ENST00000304636.9:c.1609-46dup MANE Select | ENSP00000304408.4:n.1609-46dup | |
ENST00000304636.7:c.1609-46dup | ENSP00000304408.3:n.1609-46dup | |
ENST00000317840.9:c.1609-46dup | ENSP00000315243.6:n.1609-46dup | |
NM_000090.3:c.1609-46dup , LRG_3t1:c.1609-46dup | NP_000081.1:n.1609-46dup | |
NM_000090.4:c.1609-46dup MANE Select | NP_000081.2:n.1609-46dup |