Canonical Allele Identifier: CA2398889610

Gene: MYO18B

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.25777694T= , CM000684.2:g.25777694T=	GRCh38
NC_000022.10:g.26173661T= , CM000684.1:g.26173661T=	GRCh37
NC_000022.9:g.24503661T=	NCBI36
NG_046772.1:g.40551T=

Transcript Alleles

HGVS	Amino-acid Change
NM_032608.7:c.1981T= MANE Select	NP_115997.5:p.Trp661=
ENST00000335473.12:c.1981T= MANE Select	ENSP00000334563.8:p.Trp661=
NM_001318245.1:c.1981T=	NP_001305174.1:p.Trp661=
NM_001318245.2:c.1981T=	NP_001305174.1:p.Trp661=
NM_032608.5:c.1981T=	NP_115997.5:p.Trp661=
NM_032608.6:c.1981T=	NP_115997.5:p.Trp661=
ENST00000335473.11:c.1981T=	ENSP00000334563.7:p.Trp661=
ENST00000407587.6:c.1981T=	ENSP00000386096.2:p.Trp661=
ENST00000418374.6:n.552T=
ENST00000536101.5:c.1981T=	ENSP00000441229.1:p.Trp661=
ENST00000539302.5:c.1981T=	ENSP00000437587.1:p.Trp661=
XM_005261786.3:c.1981T=	XP_005261843.1:p.Trp661=
XM_011530458.1:c.2107T=	XP_011528760.1:p.Trp703=
XM_011530458.2:c.2107T=	XP_011528760.1:p.Trp703=
XM_011530459.1:c.2107T=	XP_011528761.1:p.Trp703=
XM_011530459.2:c.2107T=	XP_011528761.1:p.Trp703=
XM_011530460.1:c.2107T=	XP_011528762.1:p.Trp703=
XM_011530460.2:c.2107T=	XP_011528762.1:p.Trp703=
XM_011530461.1:c.2107T=	XP_011528763.1:p.Trp703=
XM_011530461.2:c.2107T=	XP_011528763.1:p.Trp703=
XM_011530462.1:c.2107T=	XP_011528764.1:p.Trp703=
XM_011530463.1:c.2107T=	XP_011528765.1:p.Trp703=
XM_011530464.1:c.2107T=	XP_011528766.1:p.Trp703=
XM_011530464.2:c.2107T=	XP_011528766.1:p.Trp703=
XM_011530465.1:c.1624T=	XP_011528767.1:p.Trp542=
XM_011530465.2:c.1624T=	XP_011528767.1:p.Trp542=
XM_011530466.1:c.2107T=	XP_011528768.1:p.Trp703=
XM_011530466.2:c.2107T=	XP_011528768.1:p.Trp703=
XM_011530467.1:c.2107T=	XP_011528769.1:p.Trp703=
XM_017029012.1:c.2107T=	XP_016884501.1:p.Trp703=
XM_017029013.1:c.2107T=	XP_016884502.1:p.Trp703=
XM_017029014.1:c.2107T=	XP_016884503.1:p.Trp703=
XM_017029015.1:c.1981T=	XP_016884504.1:p.Trp661=
XM_017029017.1:c.-413T=	XP_016884506.1:n.-413T=