HGVS | Genome Assembly |
---|---|
NC_000020.11:g.44115730C>G , CM000682.2:g.44115730C>G | GRCh38 |
NC_000020.10:g.42744370C>G , CM000682.1:g.42744370C>G | GRCh37 |
NC_000020.9:g.42177784C>G | NCBI36 |
NG_031867.1:g.76849G>C , LRG_394:g.76849G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372980.4:c.1945G>C MANE Select | ENSP00000362071.3:p.Gly649Arg | |
ENST00000372980.3:c.1945G>C | ENSP00000362071.3:p.Gly649Arg | |
NM_020433.4:c.1945G>C , LRG_394t1:c.1945G>C | NP_065166.2:p.Gly649Arg | |
XM_006723832.2:c.1945G>C | XP_006723895.1:p.Gly649Arg | |
NM_020433.5:c.1945G>C MANE Select | NP_065166.2:p.Gly649Arg |