HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88007650_88007651insTGCATCGCCACCTCCCC , CM000666.2:g.88007650_88007651insTGCATCGCCACCTCCCC | GRCh38 |
NC_000004.11:g.88928802_88928803insTGCATCGCCACCTCCCC , CM000666.1:g.88928802_88928803insTGCATCGCCACCTCCCC | GRCh37 |
NC_000004.10:g.89147826_89147827insTGCATCGCCACCTCCCC | NCBI36 |
NG_008604.1:g.4983_4984insTGCATCGCCACCTCCCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.-84_-83insTGCATCGCCACCTCCCC MANE Select | ENSP00000237596.2:n.-84_-83insTGCATCGCCACCTCCCC | |
NM_000297.3:c.-84_-83insTGCATCGCCACCTCCCC | NP_000288.1:n.-84_-83insTGCATCGCCACCTCCCC | |
XM_011532028.1:c.-84_-83insTGCATCGCCACCTCCCC | XP_011530330.1:n.-84_-83insTGCATCGCCACCTCCCC | |
XR_244632.2:n.12_13insTGCATCGCCACCTCCCC | ||
NR_156488.1:n.4_5insTGCATCGCCACCTCCCC | ||
NM_000297.4:c.-84_-83insTGCATCGCCACCTCCCC MANE Select | NP_000288.1:n.-84_-83insTGCATCGCCACCTCCCC | |
NR_156488.2:n.16_17insTGCATCGCCACCTCCCC |