HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3154752A>C , CM000668.2:g.3154752A>C | GRCh38 |
NC_000006.11:g.3154986A>C , CM000668.1:g.3154986A>C | GRCh37 |
NC_000006.10:g.3099985A>C | NCBI36 |
NG_042223.1:g.7798T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000333628.4:c.449T>G MANE Select | ENSP00000369703.2:p.Leu150Arg | |
ENST00000679400.1:n.505T>G | ||
ENST00000679907.1:n.837T>G | ||
ENST00000680036.1:n.1231T>G | ||
ENST00000680967.1:n.1539T>G | ||
ENST00000333628.3:c.449T>G | ENSP00000369703.2:p.Leu150Arg | |
ENST00000489942.1:n.644T>G | ||
NM_001069.2:c.449T>G | NP_001060.1:p.Leu150Arg | |
NM_001310315.1:c.194T>G | NP_001297244.1:p.Leu65Arg | |
NM_001069.3:c.449T>G MANE Select | NP_001060.1:p.Leu150Arg | |
NM_001310315.2:c.194T>G | NP_001297244.1:p.Leu65Arg |