HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31635198C= , CM000668.2:g.31635198C= | GRCh38 |
NC_000006.11:g.31602975C= , CM000668.1:g.31602975C= | GRCh37 |
NC_000006.10:g.31710954C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376033.3:c.5227C= MANE Select | ENSP00000365201.2:p.Arg1743= | |
ENST00000376007.8:c.5227C= | ENSP00000365175.4:p.Arg1743= | |
ENST00000376033.2:c.5227C= | ENSP00000365201.2:p.Arg1743= | |
ENST00000484787.1:n.638C= | ||
NM_004638.3:c.5227C= | NP_004629.3:p.Arg1743= | |
NM_080686.2:c.5227C= | NP_542417.2:p.Arg1743= | |
XM_011514890.1:c.5227C= | XP_011513192.1:p.Arg1743= | |
XM_017011274.1:c.5227C= | XP_016866763.1:p.Arg1743= | |
NM_004638.4:c.5227C= MANE Select | NP_004629.3:p.Arg1743= | |
NM_080686.3:c.5227C= | NP_542417.2:p.Arg1743= |