HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140114649C>A , CM000667.2:g.140114649C>A | GRCh38 |
NC_000005.9:g.139494234C>A , CM000667.1:g.139494234C>A | GRCh37 |
NC_000005.8:g.139474418C>A | NCBI36 |
NG_041813.1:g.5527C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331327.5:c.468C>A MANE Select | ENSP00000332706.3:p.Tyr156Ter | |
ENST00000651386.1:c.468C>A | ENSP00000499133.1:p.Tyr156Ter | |
ENST00000331327.4:c.468C>A | ENSP00000332706.3:p.Tyr156Ter | |
NM_005859.4:c.468C>A | NP_005850.1:p.Tyr156Ter | |
NM_005859.5:c.468C>A MANE Select | NP_005850.1:p.Tyr156Ter |