HGVS | Genome Assembly |
---|---|
NC_000001.11:g.147908153C>A , CM000663.2:g.147908153C>A | GRCh38 |
NC_000001.10:g.147380280C>A , CM000663.1:g.147380280C>A | GRCh37 |
NC_000001.9:g.145846904C>A | NCBI36 |
NG_016242.1:g.10335C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369235.2:c.198C>A MANE Select | ENSP00000358238.1:p.Tyr66Ter | |
ENST00000369235.1:c.198C>A | ENSP00000358238.1:p.Tyr66Ter | |
NM_005267.4:c.198C>A | NP_005258.2:p.Tyr66Ter | |
XM_011509416.1:c.198C>A | XP_011507718.1:p.Tyr66Ter | |
XM_011509417.1:c.198C>A | XP_011507719.1:p.Tyr66Ter | |
XM_011509417.2:c.198C>A | XP_011507719.1:p.Tyr66Ter | |
XR_002956281.1:n.1113C>A | ||
NM_005267.5:c.198C>A MANE Select | NP_005258.2:p.Tyr66Ter |