HGVS | Genome Assembly |
---|---|
NC_000007.14:g.95324308_95324309insC , CM000669.2:g.95324308_95324309insC | GRCh38 |
NC_000007.13:g.94953620_94953621insC , CM000669.1:g.94953620_94953621insC | GRCh37 |
NC_000007.12:g.94791556_94791557insC | NCBI36 |
NG_008779.1:g.5264_5265insG | |
NG_008779.2:g.5398_5399insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222381.8:c.74+93_74+94insG MANE Select | ENSP00000222381.3:n.74+93_74+94insG | |
ENST00000222381.7:c.74+93_74+94insG | ENSP00000222381.3:n.74+93_74+94insG | |
ENST00000433729.1:c.74+93_74+94insG | ENSP00000407359.1:n.74+93_74+94insG | |
NM_000446.5:c.74+93_74+94insG | NP_000437.3:n.74+93_74+94insG | |
NM_000446.6:c.74+93_74+94insG | NP_000437.3:n.74+93_74+94insG | |
NM_000446.7:c.74+93_74+94insG MANE Select | NP_000437.3:n.74+93_74+94insG |