HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23433558_23433559insCC , CM000676.2:g.23433558_23433559insCC | GRCh38 |
NC_000014.8:g.23902767_23902768insCC , CM000676.1:g.23902767_23902768insCC | GRCh37 |
NC_000014.7:g.22972607_22972608insCC | NCBI36 |
NG_007884.1:g.7104_7105insGG , LRG_384:g.7104_7105insGG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000355349.4:c.175_176insGG MANE Select | ENSP00000347507.3:p.Val59GlyfsTer12 | |
ENST00000355349.3:c.175_176insGG | ENSP00000347507.3:p.Val59GlyfsTer12 | |
NM_000257.3:c.175_176insGG | NP_000248.2:p.Val59GlyfsTer12 | |
XR_245686.3:n.281_282insGG | ||
XM_017021340.1:c.175_176insGG | XP_016876829.1:p.Val59GlyfsTer12 | |
NM_000257.4:c.175_176insGG MANE Select | NP_000248.2:p.Val59GlyfsTer12 |