HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55039951C>G , CM000663.2:g.55039951C>G | GRCh38 |
NC_000001.10:g.55505624C>G , CM000663.1:g.55505624C>G | GRCh37 |
NC_000001.9:g.55278212C>G | NCBI36 |
NG_009061.1:g.5405C>G , LRG_275:g.5405C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000673913.2:c.114C>G | ENSP00000501161.2:p.Tyr38Ter | |
ENST00000710286.1:c.471C>G | ENSP00000518176.1:p.Tyr157Ter | |
ENST00000673726.1:c.114C>G | ENSP00000501004.1:p.Tyr38Ter | |
ENST00000302118.5:c.114C>G MANE Select | ENSP00000303208.5:p.Tyr38Ter | |
NM_174936.3:c.114C>G , LRG_275t1:c.114C>G | NP_777596.2:p.Tyr38Ter | |
NM_174936.4:c.114C>G MANE Select | NP_777596.2:p.Tyr38Ter |