HGVS | Genome Assembly |
---|---|
NC_000001.11:g.68429918A>C , CM000663.2:g.68429918A>C | GRCh38 |
NC_000001.10:g.68895601A>C , CM000663.1:g.68895601A>C | GRCh37 |
NC_000001.9:g.68668189A>C | NCBI36 |
NG_008472.1:g.25042T>G | |
NG_008472.2:g.25042T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262340.6:c.1460T>G MANE Select | ENSP00000262340.5:p.Leu487Arg | |
ENST00000262340.5:c.1460T>G | ENSP00000262340.5:p.Leu487Arg | |
NM_000329.2:c.1460T>G | NP_000320.1:p.Leu487Arg | |
XM_017002027.1:c.1184T>G | XP_016857516.1:p.Leu395Arg | |
NM_000329.3:c.1460T>G MANE Select | NP_000320.1:p.Leu487Arg |