HGVS | Genome Assembly |
---|---|
NC_000019.10:g.2274815_2274816insT , CM000681.2:g.2274815_2274816insT | GRCh38 |
NC_000019.9:g.2274814_2274815insT , CM000681.1:g.2274814_2274815insT | GRCh37 |
NC_000019.8:g.2225814_2225815insT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000342063.5:c.*864_*865insA MANE Select | ENSP00000345102.3:n.*864_*865insA | |
ENST00000342063.4:c.*864_*865insA | ENSP00000345102.3:n.*864_*865insA | |
ENST00000621615.1:c.146+5071_146+5072insT | ENSP00000481965.1:n.146+5071_146+5072insT | |
NM_198532.2:c.*864_*865insA | NP_940934.1:n.*864_*865insA | |
NM_198532.3:c.*864_*865insA MANE Select | NP_940934.1:n.*864_*865insA |