HGVS | Genome Assembly |
---|---|
NC_000001.11:g.119421923A>G , CM000663.2:g.119421923A>G | GRCh38 |
NC_000001.10:g.119964546A>G , CM000663.1:g.119964546A>G | GRCh37 |
NC_000001.9:g.119766069A>G | NCBI36 |
NG_013349.1:g.11993A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369416.4:c.422A>G MANE Select | ENSP00000358424.3:p.His141Arg | |
ENST00000369416.3:c.422A>G | ENSP00000358424.3:p.His141Arg | |
ENST00000433745.5:c.422A>G | ENSP00000388292.1:p.His141Arg | |
ENST00000448448.2:n.366A>G | ||
ENST00000543831.5:c.422A>G | ENSP00000445122.1:p.His141Arg | |
NM_000198.3:c.422A>G | NP_000189.1:p.His141Arg | |
NM_001166120.1:c.422A>G | NP_001159592.1:p.His141Arg | |
NM_000198.4:c.422A>G MANE Select | NP_000189.1:p.His141Arg | |
NM_001166120.2:c.422A>G | NP_001159592.1:p.His141Arg |