HGVS | Genome Assembly |
---|---|
NC_000018.10:g.22181437_22181438delinsCT , CM000680.2:g.22181437_22181438delinsCT | GRCh38 |
NC_000018.9:g.19761398_19761399delinsCT , CM000680.1:g.19761398_19761399delinsCT | GRCh37 |
NC_000018.8:g.18015396_18015397delinsCT | NCBI36 |
NG_032677.1:g.16995_16996delinsCT | |
NG_032677.2:g.17001_17002delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000269216.10:c.1303-16_1303-15delinsCT MANE Select | ENSP00000269216.3:n.1303-16_1303-15delinsCT | |
ENST00000269216.7:c.1303-16_1303-15delinsCT | ENSP00000269216.3:n.1303-16_1303-15delinsCT | |
ENST00000581694.1:c.1303-16_1303-15delinsCT | ENSP00000462313.1:n.1303-16_1303-15delinsCT | |
NM_005257.5:c.1303-16_1303-15delinsCT | NP_005248.2:n.1303-16_1303-15delinsCT | |
NM_005257.6:c.1303-16_1303-15delinsCT MANE Select | NP_005248.2:n.1303-16_1303-15delinsCT |