Canonical Allele Identifier: CA14712629

Gene: MYO9B

Genomic Alleles

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

Transcript Alleles

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