HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2445435T>C , CM000673.2:g.2445435T>C | GRCh38 |
NC_000011.9:g.2466665T>C , CM000673.1:g.2466665T>C | GRCh37 |
NC_000011.8:g.2423241T>C | NCBI36 |
NG_008935.1:g.5445T>C , LRG_287:g.5445T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000496887.7:c.76T>C | ENSP00000434560.2:p.Phe26Leu | |
ENST00000646564.2:c.337T>C | ENSP00000495806.2:p.Phe113Leu | |
ENST00000155840.12:c.337T>C MANE Select | ENSP00000155840.2:p.Phe113Leu | |
ENST00000155840.9:c.337T>C | ENSP00000155840.2:p.Phe113Leu | |
ENST00000345015.4:n.114T>C | ||
ENST00000496887.6:c.76T>C | ENSP00000434560.1:p.Phe26Leu | |
NM_000218.2:c.337T>C , LRG_287t1:c.337T>C | NP_000209.2:p.Phe113Leu | |
NM_000218.3:c.337T>C MANE Select | NP_000209.2:p.Phe113Leu |