HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18786136C= , CM000681.2:g.18786136C= | GRCh38 |
NC_000019.9:g.18896946C= , CM000681.1:g.18896946C= | GRCh37 |
NC_000019.8:g.18757946C= | NCBI36 |
NG_007070.1:g.10169G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.1318G= MANE Select | ENSP00000222271.2:p.Gly440= | |
ENST00000222271.6:c.1318G= | ENSP00000222271.2:p.Gly440= | |
ENST00000425807.1:c.1159G= | ENSP00000403792.1:p.Gly387= | |
ENST00000542601.6:c.1219G= | ENSP00000439156.2:p.Gly407= | |
ENST00000612179.1:n.568G= | ||
NM_000095.2:c.1318G= | NP_000086.2:p.Gly440= | |
NM_000095.3:c.1318G= MANE Select | NP_000086.2:p.Gly440= |