HGVS | Genome Assembly |
---|---|
NC_000020.11:g.59024068C>G , CM000682.2:g.59024068C>G | GRCh38 |
NC_000020.10:g.57599123C>G , CM000682.1:g.57599123C>G | GRCh37 |
NC_000020.9:g.57032518C>G | NCBI36 |
NG_023424.2:g.9815C>G , LRG_581:g.9815C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217133.2:c.641C>G MANE Select | ENSP00000217133.1:p.Thr214Ser | |
ENST00000217133.1:c.641C>G | ENSP00000217133.1:p.Thr214Ser | |
NM_030773.3:c.641C>G , LRG_581t1:c.641C>G | NP_110400.1:p.Thr214Ser | |
XM_017028085.1:c.575C>G | XP_016883574.1:p.Thr192Ser | |
NM_030773.4:c.641C>G MANE Select | NP_110400.1:p.Thr214Ser |