Canonical Allele Identifier: CA2398995607

Gene: MYO18B

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26007539G= , CM000684.2:g.26007539G=	GRCh38
NC_000022.10:g.26403505G= , CM000684.1:g.26403505G=	GRCh37
NC_000022.9:g.24733505G=	NCBI36
NG_046772.1:g.270396G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000335473.12:c.6470+2684G= MANE Select	ENSP00000334563.8:n.6470+2684G=
ENST00000335473.11:c.6470+2684G=	ENSP00000334563.7:n.6470+2684G=
ENST00000407587.6:c.6473+2684G=	ENSP00000386096.2:n.6473+2684G=
ENST00000418374.6:n.5041+2684G=
ENST00000536101.5:c.6470+2684G=	ENSP00000441229.1:n.6470+2684G=
ENST00000539302.5:c.*3928+2684G=	ENSP00000437587.1:n.*3928+2684G=
ENST00000543971.1:c.319+2684G=
NM_032608.5:c.6470+2684G=	NP_115997.5:n.6470+2684G=
XM_005261786.3:c.6473+2684G=	XP_005261843.1:n.6473+2684G=
XM_011530458.1:c.6599+2684G=	XP_011528760.1:n.6599+2684G=
XM_011530459.1:c.6599+2684G=	XP_011528761.1:n.6599+2684G=
XM_011530460.1:c.6599+2684G=	XP_011528762.1:n.6599+2684G=
XM_011530461.1:c.6599+2684G=	XP_011528763.1:n.6599+2684G=
XM_011530462.1:c.6599+2684G=	XP_011528764.1:n.6599+2684G=
XM_011530463.1:c.6599+2684G=	XP_011528765.1:n.6599+2684G=
XM_011530464.1:c.6596+2684G=	XP_011528766.1:n.6596+2684G=
XM_011530465.1:c.6116+2684G=	XP_011528767.1:n.6116+2684G=
NM_001318245.1:c.6473+2684G=	NP_001305174.1:n.6473+2684G=
NM_032608.6:c.6470+2684G=	NP_115997.5:n.6470+2684G=
XM_011530458.2:c.6599+2684G=	XP_011528760.1:n.6599+2684G=
XM_011530459.2:c.6599+2684G=	XP_011528761.1:n.6599+2684G=
XM_011530460.2:c.6599+2684G=	XP_011528762.1:n.6599+2684G=
XM_011530461.2:c.6599+2684G=	XP_011528763.1:n.6599+2684G=
XM_011530464.2:c.6596+2684G=	XP_011528766.1:n.6596+2684G=
XM_011530465.2:c.6116+2684G=	XP_011528767.1:n.6116+2684G=
XM_017029012.1:c.6599+2684G=	XP_016884501.1:n.6599+2684G=
XM_017029013.1:c.6599+2684G=	XP_016884502.1:n.6599+2684G=
XM_017029014.1:c.6596+2684G=	XP_016884503.1:n.6596+2684G=
XM_017029015.1:c.6467+2684G=	XP_016884504.1:n.6467+2684G=
XM_017029016.1:c.3935+2684G=	XP_016884505.1:n.3935+2684G=
XM_017029017.1:c.3932+2684G=	XP_016884506.1:n.3932+2684G=
NM_001318245.2:c.6473+2684G=	NP_001305174.1:n.6473+2684G=
NM_032608.7:c.6470+2684G= MANE Select	NP_115997.5:n.6470+2684G=