Canonical Allele Identifier: CA1306932800

Gene: MYO3B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.170509403T= , CM000664.2:g.170509403T=	GRCh38
NC_000002.11:g.171365913T= , CM000664.1:g.171365913T=	GRCh37
NC_000002.10:g.171074159T=	NCBI36
NG_034020.1:g.336259T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000408978.9:c.3371-5518T= MANE Select	ENSP00000386213.4:n.3371-5518T=
ENST00000317935.10:c.3290-5518T=	ENSP00000314650.6:n.3290-5518T=
ENST00000408978.8:c.3371-5518T=	ENSP00000386213.4:n.3371-5518T=
ENST00000409044.7:c.3290-5518T=	ENSP00000386497.3:n.3290-5518T=
ENST00000409940.6:n.3514-5518T=
ENST00000438642.6:n.3514-5518T=
ENST00000602629.1:n.2599-5518T=
NM_001083615.3:c.3290-5518T=	NP_001077084.2:n.3290-5518T=
NM_138995.4:c.3371-5518T=	NP_620482.3:n.3371-5518T=
NR_045682.1:n.3514-5518T=
NR_045683.1:n.3514-5518T=
NR_045684.1:n.3433-5518T=
XM_006712299.2:c.3398-5518T=	XP_006712362.1:n.3398-5518T=
XM_011510654.1:c.3398-5518T=	XP_011508956.1:n.3398-5518T=
XM_011510655.1:c.3317-5518T=	XP_011508957.1:n.3317-5518T=
XM_011510656.1:c.2705-5518T=	XP_011508958.1:n.2705-5518T=
XM_011510657.1:c.2390-5518T=	XP_011508959.1:n.2390-5518T=
XM_011510658.1:c.2390-5518T=	XP_011508960.1:n.2390-5518T=
XM_006712299.4:c.3398-5518T=	XP_006712362.1:n.3398-5518T=
XM_011510654.3:c.3398-5518T=	XP_011508956.1:n.3398-5518T=
XM_011510655.3:c.3317-5518T=	XP_011508957.1:n.3317-5518T=
XM_011510656.3:c.2705-5518T=	XP_011508958.1:n.2705-5518T=
XM_011510657.3:c.2390-5518T=	XP_011508959.1:n.2390-5518T=
XM_011510658.3:c.2390-5518T=	XP_011508960.1:n.2390-5518T=
XM_024452713.1:c.2390-5518T=	XP_024308481.1:n.2390-5518T=
NM_001083615.4:c.3290-5518T=	NP_001077084.2:n.3290-5518T=
NM_138995.5:c.3371-5518T= MANE Select	NP_620482.3:n.3371-5518T=
NR_045682.2:n.3512-5518T=
NR_045683.2:n.3512-5518T=
NR_045684.2:n.3431-5518T=