HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990512_45990513del , CM000683.2:g.45990512_45990513del | GRCh38 |
NC_000021.8:g.47410426_47410427del , CM000683.1:g.47410426_47410427del | GRCh37 |
NC_000021.7:g.46234854_46234855del | NCBI36 |
NG_008674.1:g.13764_13765del , LRG_475:g.13764_13765del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+90_1002+91del MANE Select | ENSP00000355180.3:n.1002+90_1002+91del | |
ENST00000361866.7:c.1002+90_1002+91del | ENSP00000355180.3:n.1002+90_1002+91del | |
ENST00000612273.1:c.1002+90_1002+91del | ENSP00000483630.1:n.1002+90_1002+91del | |
NM_001848.2:c.1002+90_1002+91del , LRG_475t1:c.1002+90_1002+91del | NP_001839.2:n.1002+90_1002+91del | |
NM_001848.3:c.1002+90_1002+91del MANE Select | NP_001839.2:n.1002+90_1002+91del |