HGVS | Genome Assembly |
---|---|
NC_000010.11:g.114043927_114043944dup , CM000672.2:g.114043927_114043944dup | GRCh38 |
NC_000010.10:g.115803686_115803703dup , CM000672.1:g.115803686_115803703dup | GRCh37 |
NC_000010.9:g.115793676_115793693dup | NCBI36 |
NG_012187.1:g.4881_4898dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369295.4:c.-206_-189dup MANE Select | ENSP00000358301.2:n.-206_-189dup | |
NM_000684.3:c.-206_-189dup MANE Select | NP_000675.1:n.-206_-189dup |