HGVS | Genome Assembly |
---|---|
NC_000017.11:g.40866966C= , CM000679.2:g.40866966C= | GRCh38 |
NC_000017.10:g.39023218C= , CM000679.1:g.39023218C= | GRCh37 |
NC_000017.9:g.36276744C= | NCBI36 |
NG_008077.1:g.5245G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000251643.5:c.221G= MANE Select | ENSP00000251643.4:p.Gly74= | |
ENST00000647902.1:c.211+10G= | ENSP00000497770.1:n.211+10G= | |
ENST00000251643.4:c.221G= | ENSP00000251643.4:p.Gly74= | |
NM_000223.3:c.221G= | NP_000214.1:p.Gly74= | |
XR_934754.1:n.1500+16106C= | ||
XR_934754.2:n.2008+16106C= | ||
NM_000223.4:c.221G= MANE Select | NP_000214.1:p.Gly74= |