HGVS | Genome Assembly |
---|---|
NC_000006.12:g.151526735_151526736delinsAT , CM000668.2:g.151526735_151526736delinsAT | GRCh38 |
NC_000006.11:g.151847870_151847871delinsAT , CM000668.1:g.151847870_151847871delinsAT | GRCh37 |
NC_000006.10:g.151889563_151889564delinsAT | NCBI36 |
NG_021198.1:g.37696_37697delinsAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000239374.8:c.58-9583_58-9582delinsAT MANE Select | ENSP00000239374.6:n.58-9583_58-9582delins... | |
ENST00000239374.7:c.58-9583_58-9582delinsAT | ENSP00000239374.6:n.58-9583_58-9582delins... | |
NM_025059.3:c.58-9583_58-9582delinsAT | NP_079335.2:n.58-9583_58-9582delinsAT | |
NM_025059.4:c.58-9583_58-9582delinsAT MANE Select | NP_079335.2:n.58-9583_58-9582delinsAT |