HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45990556_45990557insT , CM000683.2:g.45990556_45990557insT | GRCh38 |
NC_000021.8:g.47410470_47410471insT , CM000683.1:g.47410470_47410471insT | GRCh37 |
NC_000021.7:g.46234898_46234899insT | NCBI36 |
NG_008674.1:g.13808_13809insT , LRG_475:g.13808_13809insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.1002+134_1002+135insT MANE Select | ENSP00000355180.3:n.1002+134_1002+135insT | |
ENST00000361866.7:c.1002+134_1002+135insT | ENSP00000355180.3:n.1002+134_1002+135insT | |
ENST00000612273.1:c.1002+134_1002+135insT | ENSP00000483630.1:n.1002+134_1002+135insT | |
NM_001848.2:c.1002+134_1002+135insT , LRG_475t1:c.1002+134_1002+135insT | NP_001839.2:n.1002+134_1002+135insT | |
NM_001848.3:c.1002+134_1002+135insT MANE Select | NP_001839.2:n.1002+134_1002+135insT |