HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177992766_177992767insGGGGCTGGGGGGGGGGGGGGGGG , CM000667.2:g.177992766_177992767insGGGGCTGGGGGGGGGGGGGGGGG | GRCh38 |
NC_000005.9:g.177419767_177419768insGGGGCTGGGGGGGGGGGGGGGGG , CM000667.1:g.177419767_177419768insGGGGCTGGGGGGGGGGGGGGGGG | GRCh37 |
NC_000005.8:g.177352373_177352374insGGGGCTGGGGGGGGGGGGGGGGG | NCBI36 |
NG_015889.1:g.8482_8483insCCCCCCCCCCCAGCCCCCCCCCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308304.2:c.629_630insCCCCCCCCCCCAGCCCCCCCCCC MANE Select | ENSP00000311290.2:p.Met214GlnfsTer30 | |
NM_006261.4:c.629_630insCCCCCCCCCCCAGCCCCCCCCCC | NP_006252.3:p.Met214GlnfsTer30 | |
NM_006261.5:c.629_630insCCCCCCCCCCCAGCCCCCCCCCC MANE Select | NP_006252.4:p.Met214GlnfsTer30 |