Canonical Allele Identifier: CA751957642

Gene: MYO18B

Linked Data

• dbSNP Id: rs1395106567
• MyVariant Identifiers: chr22:g.26403538A>G (hg19) ; chr22:g.26007572A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26007572A>G , CM000684.2:g.26007572A>G	GRCh38
NC_000022.10:g.26403538A>G , CM000684.1:g.26403538A>G	GRCh37
NC_000022.9:g.24733538A>G	NCBI36
NG_046772.1:g.270429A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000335473.12:c.6470+2717A>G MANE Select	ENSP00000334563.8:n.6470+2717A>G
ENST00000335473.11:c.6470+2717A>G	ENSP00000334563.7:n.6470+2717A>G
ENST00000407587.6:c.6473+2717A>G	ENSP00000386096.2:n.6473+2717A>G
ENST00000418374.6:n.5041+2717A>G
ENST00000536101.5:c.6470+2717A>G	ENSP00000441229.1:n.6470+2717A>G
ENST00000539302.5:c.*3928+2717A>G	ENSP00000437587.1:n.*3928+2717A>G
ENST00000543971.1:c.319+2717A>G
NM_032608.5:c.6470+2717A>G	NP_115997.5:n.6470+2717A>G
XM_005261786.3:c.6473+2717A>G	XP_005261843.1:n.6473+2717A>G
XM_011530458.1:c.6599+2717A>G	XP_011528760.1:n.6599+2717A>G
XM_011530459.1:c.6599+2717A>G	XP_011528761.1:n.6599+2717A>G
XM_011530460.1:c.6599+2717A>G	XP_011528762.1:n.6599+2717A>G
XM_011530461.1:c.6599+2717A>G	XP_011528763.1:n.6599+2717A>G
XM_011530462.1:c.6599+2717A>G	XP_011528764.1:n.6599+2717A>G
XM_011530463.1:c.6599+2717A>G	XP_011528765.1:n.6599+2717A>G
XM_011530464.1:c.6596+2717A>G	XP_011528766.1:n.6596+2717A>G
XM_011530465.1:c.6116+2717A>G	XP_011528767.1:n.6116+2717A>G
NM_001318245.1:c.6473+2717A>G	NP_001305174.1:n.6473+2717A>G
NM_032608.6:c.6470+2717A>G	NP_115997.5:n.6470+2717A>G
XM_011530458.2:c.6599+2717A>G	XP_011528760.1:n.6599+2717A>G
XM_011530459.2:c.6599+2717A>G	XP_011528761.1:n.6599+2717A>G
XM_011530460.2:c.6599+2717A>G	XP_011528762.1:n.6599+2717A>G
XM_011530461.2:c.6599+2717A>G	XP_011528763.1:n.6599+2717A>G
XM_011530464.2:c.6596+2717A>G	XP_011528766.1:n.6596+2717A>G
XM_011530465.2:c.6116+2717A>G	XP_011528767.1:n.6116+2717A>G
XM_017029012.1:c.6599+2717A>G	XP_016884501.1:n.6599+2717A>G
XM_017029013.1:c.6599+2717A>G	XP_016884502.1:n.6599+2717A>G
XM_017029014.1:c.6596+2717A>G	XP_016884503.1:n.6596+2717A>G
XM_017029015.1:c.6467+2717A>G	XP_016884504.1:n.6467+2717A>G
XM_017029016.1:c.3935+2717A>G	XP_016884505.1:n.3935+2717A>G
XM_017029017.1:c.3932+2717A>G	XP_016884506.1:n.3932+2717A>G
NM_001318245.2:c.6473+2717A>G	NP_001305174.1:n.6473+2717A>G
NM_032608.7:c.6470+2717A>G MANE Select	NP_115997.5:n.6470+2717A>G