HGVS | Genome Assembly |
---|---|
NC_000019.10:g.2274948_2274949insG , CM000681.2:g.2274948_2274949insG | GRCh38 |
NC_000019.9:g.2274947_2274948insG , CM000681.1:g.2274947_2274948insG | GRCh37 |
NC_000019.8:g.2225947_2225948insG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000342063.5:c.*731_*732insC MANE Select | ENSP00000345102.3:n.*731_*732insC | |
ENST00000342063.4:c.*731_*732insC | ENSP00000345102.3:n.*731_*732insC | |
ENST00000621615.1:c.146+5204_146+5205insG | ENSP00000481965.1:n.146+5204_146+5205insG | |
NM_198532.2:c.*731_*732insC | NP_940934.1:n.*731_*732insC | |
NM_198532.3:c.*731_*732insC MANE Select | NP_940934.1:n.*731_*732insC |