HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135833176_135833178delinsCAG , CM000664.2:g.135833176_135833178delinsCAG | GRCh38 |
NC_000002.11:g.136590746_136590748delinsCAG , CM000664.1:g.136590746_136590748delinsCAG | GRCh37 |
NC_000002.10:g.136307216_136307218delinsCAG | NCBI36 |
NG_008104.2:g.26992_26994delinsCTG , LRG_338:g.26992_26994delinsCTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264162.7:c.653_655delinsCTG MANE Select | ENSP00000264162.2:p.Ser218= | |
ENST00000264162.6:c.653_655delinsCTG | ENSP00000264162.2:p.Ser218= | |
NM_002299.2:c.653_655delinsCTG , LRG_338t1:c.653_655delinsCTG | NP_002290.2:p.Ser218= | |
NM_002299.3:c.653_655delinsCTG | NP_002290.2:p.Ser218= | |
XM_017004088.2:c.653_655delinsCTG | XP_016859577.1:p.Ser218= | |
NM_002299.4:c.653_655delinsCTG MANE Select | NP_002290.2:p.Ser218= |