HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990484_45990485insT , CM000683.2:g.45990484_45990485insT | GRCh38 |
NC_000021.8:g.47410398_47410399insT , CM000683.1:g.47410398_47410399insT | GRCh37 |
NC_000021.7:g.46234826_46234827insT | NCBI36 |
NG_008674.1:g.13736_13737insT , LRG_475:g.13736_13737insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+62_1002+63insT MANE Select | ENSP00000355180.3:n.1002+62_1002+63insT | |
ENST00000361866.7:c.1002+62_1002+63insT | ENSP00000355180.3:n.1002+62_1002+63insT | |
ENST00000612273.1:c.1002+62_1002+63insT | ENSP00000483630.1:n.1002+62_1002+63insT | |
NM_001848.2:c.1002+62_1002+63insT , LRG_475t1:c.1002+62_1002+63insT | NP_001839.2:n.1002+62_1002+63insT | |
NM_001848.3:c.1002+62_1002+63insT MANE Select | NP_001839.2:n.1002+62_1002+63insT |