HGVS | Genome Assembly |
---|---|
NC_000001.11:g.182586250A>C , CM000663.2:g.182586250A>C | GRCh38 |
NC_000001.10:g.182555385A>C , CM000663.1:g.182555385A>C | GRCh37 |
NC_000001.9:g.180822008A>C | NCBI36 |
NG_009024.2:g.5724T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367559.7:c.557T>G MANE Select | ENSP00000356530.3:p.Ile186Ser | |
ENST00000539397.1:c.557T>G | ENSP00000440844.1:p.Ile186Ser | |
NM_021133.3:c.557T>G | NP_066956.1:p.Ile186Ser | |
XM_005245411.2:c.557T>G | XP_005245468.1:p.Ile186Ser | |
XR_001737359.1:n.840T>G | ||
XR_001737360.1:n.840T>G | ||
NM_021133.4:c.557T>G MANE Select | NP_066956.1:p.Ile186Ser |