HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94942309G= , CM000672.2:g.94942309G= | GRCh38 |
NC_000010.10:g.96702066G= , CM000672.1:g.96702066G= | GRCh37 |
NC_000010.9:g.96692056G= | NCBI36 |
NG_008385.1:g.8652G= | |
NG_008385.2:g.9152G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.449G= MANE Select | ENSP00000260682.6:p.Arg150= | |
ENST00000643112.1:c.449G= | ENSP00000496202.1:p.Arg150= | |
ENST00000645207.1:n.602G= | ||
ENST00000260682.6:c.449G= | ENSP00000260682.6:p.Arg150= | |
ENST00000461906.1:n.474G= | ||
ENST00000473496.1:n.220G= | ||
NM_000771.3:c.449G= | NP_000762.2:p.Arg150= | |
NM_000771.4:c.449G= MANE Select | NP_000762.2:p.Arg150= |