HGVS | Genome Assembly |
---|---|
NC_000023.11:g.54465818T>C , CM000685.2:g.54465818T>C | GRCh38 |
NC_000023.10:g.54492251T>C , CM000685.1:g.54492251T>C | GRCh37 |
NC_000023.9:g.54508976T>C | NCBI36 |
NG_008054.1:g.35349A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375135.4:c.1375A>G MANE Select | ENSP00000364277.3:p.Lys459Glu | |
ENST00000375135.3:c.1375A>G | ENSP00000364277.3:p.Lys459Glu | |
NM_004463.2:c.1375A>G | NP_004454.2:p.Lys459Glu | |
NM_004463.3:c.1375A>G MANE Select | NP_004454.2:p.Lys459Glu |