HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43551610A>C , CM000681.2:g.43551610A>C | GRCh38 |
NC_000019.9:g.44055762A>C , CM000681.1:g.44055762A>C | GRCh37 |
NC_000019.8:g.48747602A>C | NCBI36 |
NG_033799.1:g.28969T>G , LRG_784:g.28969T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262887.10:c.1160T>G MANE Select | ENSP00000262887.5:p.Leu387Arg | |
ENST00000262887.9:c.1160T>G | ENSP00000262887.4:p.Leu387Arg | |
ENST00000543982.5:c.1067T>G | ENSP00000443671.1:p.Leu356Arg | |
ENST00000597811.5:c.770T>G | ||
NM_006297.2:c.1160T>G , LRG_784t1:c.1160T>G | NP_006288.2:p.Leu387Arg | |
NM_006297.3:c.1160T>G MANE Select | NP_006288.2:p.Leu387Arg |