Canonical Allele Identifier: CA10159696

Gene: MYO18B

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.25768736G>A , CM000684.2:g.25768736G>A	GRCh38
NC_000022.10:g.26164703G>A , CM000684.1:g.26164703G>A	GRCh37
NC_000022.9:g.24494703G>A	NCBI36
NG_046772.1:g.31593G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032608.7:c.820G>A MANE Select	NP_115997.5:p.Gly274Ser
ENST00000335473.12:c.820G>A MANE Select	ENSP00000334563.8:p.Gly274Ser
NM_001318245.1:c.820G>A	NP_001305174.1:p.Gly274Ser
NM_001318245.2:c.820G>A	NP_001305174.1:p.Gly274Ser
NM_032608.5:c.820G>A	NP_115997.5:p.Gly274Ser
NM_032608.6:c.820G>A	NP_115997.5:p.Gly274Ser
ENST00000335473.11:c.820G>A	ENSP00000334563.7:p.Gly274Ser
ENST00000407587.6:c.820G>A	ENSP00000386096.2:p.Gly274Ser
ENST00000536101.5:c.820G>A	ENSP00000441229.1:p.Gly274Ser
ENST00000539302.5:c.820G>A	ENSP00000437587.1:p.Gly274Ser
XM_005261786.3:c.820G>A	XP_005261843.1:p.Gly274Ser
XM_011530458.1:c.946G>A	XP_011528760.1:p.Gly316Ser
XM_011530458.2:c.946G>A	XP_011528760.1:p.Gly316Ser
XM_011530459.1:c.946G>A	XP_011528761.1:p.Gly316Ser
XM_011530459.2:c.946G>A	XP_011528761.1:p.Gly316Ser
XM_011530460.1:c.946G>A	XP_011528762.1:p.Gly316Ser
XM_011530460.2:c.946G>A	XP_011528762.1:p.Gly316Ser
XM_011530461.1:c.946G>A	XP_011528763.1:p.Gly316Ser
XM_011530461.2:c.946G>A	XP_011528763.1:p.Gly316Ser
XM_011530462.1:c.946G>A	XP_011528764.1:p.Gly316Ser
XM_011530463.1:c.946G>A	XP_011528765.1:p.Gly316Ser
XM_011530464.1:c.946G>A	XP_011528766.1:p.Gly316Ser
XM_011530464.2:c.946G>A	XP_011528766.1:p.Gly316Ser
XM_011530465.1:c.463G>A	XP_011528767.1:p.Gly155Ser
XM_011530465.2:c.463G>A	XP_011528767.1:p.Gly155Ser
XM_011530466.1:c.946G>A	XP_011528768.1:p.Gly316Ser
XM_011530466.2:c.946G>A	XP_011528768.1:p.Gly316Ser
XM_011530467.1:c.946G>A	XP_011528769.1:p.Gly316Ser
XM_017029012.1:c.946G>A	XP_016884501.1:p.Gly316Ser
XM_017029013.1:c.946G>A	XP_016884502.1:p.Gly316Ser
XM_017029014.1:c.946G>A	XP_016884503.1:p.Gly316Ser
XM_017029015.1:c.820G>A	XP_016884504.1:p.Gly274Ser
XM_017029017.1:c.-1574G>A	XP_016884506.1:n.-1574G>A