HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7502618C>G , CM000679.2:g.7502618C>G | GRCh38 |
NC_000017.10:g.7405937C>G , CM000679.1:g.7405937C>G | GRCh37 |
NC_000017.9:g.7346661C>G | NCBI36 |
NG_027747.1:g.23240C>G | |
NG_027747.2:g.23240C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000617998.6:n.3072C>G | ||
ENST00000674977.2:c.2673C>G | ENSP00000502190.2:p.Tyr891Ter | |
ENST00000576114.1:n.139C>G | ||
ENST00000617998.4:c.2673C>G | ENSP00000480158.1:p.Tyr891Ter | |
ENST00000621442.4:c.2673C>G | ENSP00000483957.1:p.Tyr891Ter | |
NM_000937.4:c.2673C>G | NP_000928.1:p.Tyr891Ter | |
NM_000937.5:c.2673C>G MANE Select | NP_000928.1:p.Tyr891Ter |