HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2445431C>A , CM000673.2:g.2445431C>A | GRCh38 |
NC_000011.9:g.2466661C>A , CM000673.1:g.2466661C>A | GRCh37 |
NC_000011.8:g.2423237C>A | NCBI36 |
NG_008935.1:g.5441C>A , LRG_287:g.5441C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000496887.7:c.72C>A | ENSP00000434560.2:p.Tyr24Ter | |
ENST00000646564.2:c.333C>A | ENSP00000495806.2:p.Tyr111Ter | |
ENST00000155840.12:c.333C>A MANE Select | ENSP00000155840.2:p.Tyr111Ter | |
ENST00000155840.9:c.333C>A | ENSP00000155840.2:p.Tyr111Ter | |
ENST00000345015.4:n.110C>A | ||
ENST00000496887.6:c.72C>A | ENSP00000434560.1:p.Tyr24Ter | |
NM_000218.2:c.333C>A , LRG_287t1:c.333C>A | NP_000209.2:p.Tyr111Ter | |
NM_000218.3:c.333C>A MANE Select | NP_000209.2:p.Tyr111Ter |