HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114714014_114714015insTT , CM000663.2:g.114714014_114714015insTT | GRCh38 |
NC_000001.10:g.115256635_115256636insTT , CM000663.1:g.115256635_115256636insTT | GRCh37 |
NC_000001.9:g.115058158_115058159insTT | NCBI36 |
NG_007572.1:g.7880_7881insAA , LRG_92:g.7880_7881insAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.112-37_112-36insAA MANE Select | ENSP00000358548.4:n.112-37_112-36insAA | |
ENST00000369535.4:c.112-37_112-36insAA | ENSP00000358548.4:n.112-37_112-36insAA | |
NM_002524.4:c.112-37_112-36insAA | NP_002515.1:n.112-37_112-36insAA | |
NM_002524.5:c.112-37_112-36insAA MANE Select | NP_002515.1:n.112-37_112-36insAA |