HGVS | Genome Assembly |
---|---|
NC_000001.11:g.68431294A>C , CM000663.2:g.68431294A>C | GRCh38 |
NC_000001.10:g.68896977A>C , CM000663.1:g.68896977A>C | GRCh37 |
NC_000001.9:g.68669565A>C | NCBI36 |
NG_008472.1:g.23666T>G | |
NG_008472.2:g.23666T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262340.6:c.1326T>G MANE Select | ENSP00000262340.5:p.Phe442Leu | |
ENST00000262340.5:c.1326T>G | ENSP00000262340.5:p.Phe442Leu | |
NM_000329.2:c.1326T>G | NP_000320.1:p.Phe442Leu | |
XM_017002027.1:c.1050T>G | XP_016857516.1:p.Phe350Leu | |
NM_000329.3:c.1326T>G MANE Select | NP_000320.1:p.Phe442Leu |