HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2583465A>G , CM000673.2:g.2583465A>G | GRCh38 |
NC_000011.9:g.2604695A>G , CM000673.1:g.2604695A>G | GRCh37 |
NC_000011.8:g.2561271A>G | NCBI36 |
NG_008935.1:g.143475A>G , LRG_287:g.143475A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000496887.7:c.691A>G | ENSP00000434560.2:p.Lys231Glu | |
ENST00000646564.2:c.508A>G | ENSP00000495806.2:p.Lys170Glu | |
ENST00000155840.12:c.952A>G MANE Select | ENSP00000155840.2:p.Lys318Glu | |
ENST00000335475.6:c.571A>G | ENSP00000334497.5:p.Lys191Glu | |
ENST00000646564.1:c.154A>G | ENSP00000495806.1:p.Lys52Glu | |
ENST00000155840.9:c.952A>G | ENSP00000155840.2:p.Lys318Glu | |
ENST00000335475.5:c.571A>G | ENSP00000334497.5:p.Lys191Glu | |
NM_000218.2:c.952A>G , LRG_287t1:c.952A>G | NP_000209.2:p.Lys318Glu | |
NM_181798.1:c.571A>G , LRG_287t2:c.571A>G | NP_861463.1:p.Lys191Glu | |
NM_000218.3:c.952A>G MANE Select | NP_000209.2:p.Lys318Glu |