HGVS | Genome Assembly |
---|---|
NC_000012.12:g.106463604T>G , CM000674.2:g.106463604T>G | GRCh38 |
NC_000012.11:g.106857382T>G , CM000674.1:g.106857382T>G | GRCh37 |
NC_000012.10:g.105381512T>G | NCBI36 |
NG_031837.1:g.110947T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000228347.9:c.2697T>G MANE Select | ENSP00000228347.4:p.Ser899Arg | |
ENST00000228347.8:c.2697T>G | ENSP00000228347.4:p.Ser899Arg | |
ENST00000539066.5:c.2523T>G | ENSP00000445721.1:p.Ser841Arg | |
NM_001160708.1:c.2523T>G | NP_001154180.1:p.Ser841Arg | |
NM_018082.5:c.2697T>G | NP_060552.4:p.Ser899Arg | |
XM_017019621.2:c.2697T>G | XP_016875110.1:p.Ser899Arg | |
NM_018082.6:c.2697T>G MANE Select | NP_060552.4:p.Ser899Arg | |
NM_001160708.2:c.2523T>G | NP_001154180.1:p.Ser841Arg |