HGVS | Genome Assembly |
---|---|
NC_000019.10:g.853364C>G , CM000681.2:g.853364C>G | GRCh38 |
NC_000019.9:g.853364C>G , CM000681.1:g.853364C>G | GRCh37 |
NC_000019.8:g.804364C>G | NCBI36 |
NG_009627.1:g.6074C>G , LRG_57:g.6074C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263621.2:c.327C>G MANE Select | ENSP00000263621.1:p.Tyr109Ter | |
ENST00000263621.1:c.327C>G | ENSP00000263621.1:p.Tyr109Ter | |
ENST00000590230.5:c.327C>G | ENSP00000466090.1:p.Tyr109Ter | |
NM_001972.2:c.327C>G , LRG_57t1:c.327C>G | NP_001963.1:p.Tyr109Ter | |
XM_011527775.1:c.327C>G | XP_011526077.1:p.Tyr109Ter | |
XM_011527776.1:c.327C>G | XP_011526078.1:p.Tyr109Ter | |
NM_001972.3:c.327C>G | NP_001963.1:p.Tyr109Ter | |
NM_001972.4:c.327C>G MANE Select | NP_001963.1:p.Tyr109Ter |