Canonical Allele Identifier: CA2399004076
Community Standard Title: NM_032608.7(MYO18B):c.6496G= (p.Glu2166=)
Gene: MYO18B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26026470G= , CM000684.2:g.26026470G= GRCh38
NC_000022.10:g.26422436G= , CM000684.1:g.26422436G= GRCh37
NC_000022.9:g.24752436G= NCBI36
NG_046772.1:g.289327G=

Transcript Alleles

HGVS Amino-acid Change
NM_032608.7:c.6496G= MANE Select NP_115997.5:p.Glu2166=
ENST00000335473.12:c.6496G= MANE Select ENSP00000334563.8:p.Glu2166=
NM_001318245.1:c.6499G= NP_001305174.1:p.Glu2167=
NM_001318245.2:c.6499G= NP_001305174.1:p.Glu2167=
NM_032608.5:c.6496G= NP_115997.5:p.Glu2166=
NM_032608.6:c.6496G= NP_115997.5:p.Glu2166=
ENST00000335473.11:c.6496G= ENSP00000334563.7:p.Glu2166=
ENST00000407587.6:c.6499G= ENSP00000386096.2:p.Glu2167=
ENST00000418374.6:n.5067G=
ENST00000536101.5:c.6496G= ENSP00000441229.1:p.Glu2166=
ENST00000539302.5:c.*3954G= ENSP00000437587.1:n.*3954G=
ENST00000543971.1:c.345G=
XM_005261786.3:c.6499G= XP_005261843.1:p.Glu2167=
XM_011530458.1:c.6625G= XP_011528760.1:p.Glu2209=
XM_011530458.2:c.6625G= XP_011528760.1:p.Glu2209=
XM_011530459.1:c.6625G= XP_011528761.1:p.Glu2209=
XM_011530459.2:c.6625G= XP_011528761.1:p.Glu2209=
XM_011530460.1:c.6625G= XP_011528762.1:p.Glu2209=
XM_011530460.2:c.6625G= XP_011528762.1:p.Glu2209=
XM_011530461.1:c.6625G= XP_011528763.1:p.Glu2209=
XM_011530461.2:c.6625G= XP_011528763.1:p.Glu2209=
XM_011530462.1:c.6625G= XP_011528764.1:p.Glu2209=
XM_011530463.1:c.6625G= XP_011528765.1:p.Glu2209=
XM_011530464.1:c.6622G= XP_011528766.1:p.Glu2208=
XM_011530464.2:c.6622G= XP_011528766.1:p.Glu2208=
XM_011530465.1:c.6142G= XP_011528767.1:p.Glu2048=
XM_011530465.2:c.6142G= XP_011528767.1:p.Glu2048=
XM_017029012.1:c.6625G= XP_016884501.1:p.Glu2209=
XM_017029013.1:c.6625G= XP_016884502.1:p.Glu2209=
XM_017029014.1:c.6622G= XP_016884503.1:p.Glu2208=
XM_017029015.1:c.6493G= XP_016884504.1:p.Glu2165=
XM_017029016.1:c.3961G= XP_016884505.1:p.Glu1321=
XM_017029017.1:c.3958G= XP_016884506.1:p.Glu1320=