Canonical Allele Identifier: CA2325738612

Gene: MYO9B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17203024G= , CM000681.2:g.17203024G=	GRCh38
NC_000019.9:g.17313833G= , CM000681.1:g.17313833G=	GRCh37
NC_000019.8:g.17174833G=	NCBI36
NG_013068.1:g.132243G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004145.4:c.4879-123G= MANE Select	NP_004136.2:n.4879-123G=
ENST00000682292.1:c.4879-123G= MANE Select	ENSP00000507803.1:n.4879-123G=
NM_001130065.1:c.4879-123G=	NP_001123537.1:n.4879-123G=
NM_001130065.2:c.4879-123G=	NP_001123537.1:n.4879-123G=
NM_004145.3:c.4879-123G=	NP_004136.2:n.4879-123G=
ENST00000397274.6:c.4879-123G=	ENSP00000380444.2:n.4879-123G=
ENST00000593533.1:n.828+141G=
ENST00000594824.5:c.4879-123G=	ENSP00000471367.1:n.4879-123G=
ENST00000595618.5:c.4879-123G=	ENSP00000471457.1:n.4879-123G=
ENST00000595641.5:c.4879-123G=	ENSP00000472915.1:n.4879-123G=
ENST00000599420.5:n.358G=
ENST00000602158.1:c.135+20G=
XM_011528029.1:c.4969-123G=	XP_011526331.1:n.4969-123G=
XM_011528030.1:c.4966-123G=	XP_011526332.1:n.4966-123G=
XM_011528031.1:c.4969-123G=	XP_011526333.1:n.4969-123G=
XM_011528032.1:c.4966-123G=	XP_011526334.1:n.4966-123G=
XM_011528033.1:c.4879-123G=	XP_011526335.1:n.4879-123G=
XM_011528034.1:c.4765-123G=	XP_011526336.1:n.4765-123G=
XM_011528035.1:c.4969-123G=	XP_011526337.1:n.4969-123G=
XM_011528037.1:c.4876-123G=	XP_011526339.1:n.4876-123G=
XM_011528038.1:c.4876-123G=	XP_011526340.1:n.4876-123G=
XR_936183.1:n.5123-123G=
XR_936184.1:n.5243+20G=
XR_936185.1:n.5240+20G=