HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20189283_20189284delinsTG , CM000675.2:g.20189283_20189284delinsTG | GRCh38 |
NC_000013.10:g.20763422_20763423delinsTG , CM000675.1:g.20763422_20763423delinsTG | GRCh37 |
NC_000013.9:g.19661422_19661423delinsTG | NCBI36 |
NG_008358.1:g.8692_8693delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.298_299delinsCA | ENSP00000372295.1:p.His100= | |
ENST00000382848.5:c.298_299delinsCA MANE Select | ENSP00000372299.4:p.His100= | |
ENST00000382844.1:c.298_299delinsCA | ENSP00000372295.1:p.His100= | |
ENST00000382848.4:c.298_299delinsCA | ENSP00000372299.4:p.His100= | |
NM_004004.5:c.298_299delinsCA | NP_003995.2:p.His100= | |
XM_011535049.1:c.298_299delinsCA | XP_011533351.1:p.His100= | |
XM_011535049.2:c.298_299delinsCA | XP_011533351.1:p.His100= | |
NM_004004.6:c.298_299delinsCA MANE Select | NP_003995.2:p.His100= |