Canonical Allele Identifier: CA2325733175

Gene: MYO9B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17191438G= , CM000681.2:g.17191438G=	GRCh38
NC_000019.9:g.17302247G= , CM000681.1:g.17302247G=	GRCh37
NC_000019.8:g.17163247G=	NCBI36
NG_013068.1:g.120657G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004145.4:c.2811+219G= MANE Select	NP_004136.2:n.2811+219G=
ENST00000682292.1:c.2811+219G= MANE Select	ENSP00000507803.1:n.2811+219G=
NM_001130065.1:c.2811+219G=	NP_001123537.1:n.2811+219G=
NM_001130065.2:c.2811+219G=	NP_001123537.1:n.2811+219G=
NM_004145.3:c.2811+219G=	NP_004136.2:n.2811+219G=
ENST00000397274.6:c.2811+219G=	ENSP00000380444.2:n.2811+219G=
ENST00000594824.5:c.2811+219G=	ENSP00000471367.1:n.2811+219G=
ENST00000595618.5:c.2811+219G=	ENSP00000471457.1:n.2811+219G=
ENST00000595641.5:c.2811+219G=	ENSP00000472915.1:n.2811+219G=
XM_011528029.1:c.2901+219G=	XP_011526331.1:n.2901+219G=
XM_011528030.1:c.2901+219G=	XP_011526332.1:n.2901+219G=
XM_011528031.1:c.2901+219G=	XP_011526333.1:n.2901+219G=
XM_011528032.1:c.2901+219G=	XP_011526334.1:n.2901+219G=
XM_011528033.1:c.2811+219G=	XP_011526335.1:n.2811+219G=
XM_011528034.1:c.2697+219G=	XP_011526336.1:n.2697+219G=
XM_011528035.1:c.2901+219G=	XP_011526337.1:n.2901+219G=
XM_011528036.1:c.2901+219G=	XP_011526338.1:n.2901+219G=
XM_011528037.1:c.2811+219G=	XP_011526339.1:n.2811+219G=
XM_011528038.1:c.2811+219G=	XP_011526340.1:n.2811+219G=
XR_936183.1:n.3055+219G=
XR_936184.1:n.3055+219G=
XR_936185.1:n.3055+219G=