HGVS | Genome Assembly |
---|---|
NC_000022.11:g.19797570C= , CM000684.2:g.19797570C= | GRCh38 |
NC_000022.10:g.19785093C= , CM000684.1:g.19785093C= | GRCh37 |
NC_000022.9:g.18165093C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000329517.11:c.732+4431G= MANE Select | ENSP00000331313.6:n.732+4431G= | |
ENST00000329517.10:c.732+4431G= | ENSP00000331313.6:n.732+4431G= | |
ENST00000403325.5:c.732+4431G= | ENSP00000385154.1:n.732+4431G= | |
ENST00000405009.5:c.630+4533G= | ENSP00000384626.1:n.630+4533G= | |
ENST00000460402.5:n.700+4431G= | ||
NM_053004.2:c.732+4431G= | NP_443730.1:n.732+4431G= | |
NM_053004.3:c.732+4431G= MANE Select | NP_443730.1:n.732+4431G= |