HGVS | Genome Assembly |
---|---|
NC_000006.12:g.49459004_49459005insCC , CM000668.2:g.49459004_49459005insCC | GRCh38 |
NC_000006.11:g.49426717_49426718insCC , CM000668.1:g.49426717_49426718insCC | GRCh37 |
NC_000006.10:g.49534676_49534677insCC | NCBI36 |
NG_007100.1:g.9135_9136insGG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274813.4:c.385+77_385+78insGG MANE Select | ENSP00000274813.3:n.385+77_385+78insGG | |
ENST00000274813.3:c.385+77_385+78insGG | ENSP00000274813.3:n.385+77_385+78insGG | |
NM_000255.3:c.385+77_385+78insGG | NP_000246.2:n.385+77_385+78insGG | |
XM_005249143.2:c.385+77_385+78insGG | XP_005249200.1:n.385+77_385+78insGG | |
XM_005249143.3:c.385+77_385+78insGG | XP_005249200.1:n.385+77_385+78insGG | |
NM_000255.4:c.385+77_385+78insGG MANE Select | NP_000246.2:n.385+77_385+78insGG |