HGVS | Genome Assembly |
---|---|
NC_000012.12:g.68158730_68158743dup , CM000674.2:g.68158730_68158743dup | GRCh38 |
NC_000012.11:g.68552510_68552523dup , CM000674.1:g.68552510_68552523dup | GRCh37 |
NC_000012.10:g.66838777_66838790dup | NCBI36 |
NG_015840.1:g.6014_6027dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000229135.4:c.115-469_115-456dup MANE Select | ENSP00000229135.3:n.115-469_115-456dup | |
ENST00000229135.3:c.115-469_115-456dup | ENSP00000229135.3:n.115-469_115-456dup | |
NM_000619.2:c.115-469_115-456dup | NP_000610.2:n.115-469_115-456dup | |
NM_000619.3:c.115-469_115-456dup MANE Select | NP_000610.2:n.115-469_115-456dup |