Canonical Allele Identifier: CA404668257

Gene: MYO9B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17172867G>A , CM000681.2:g.17172867G>A	GRCh38
NC_000019.9:g.17283676G>A , CM000681.1:g.17283676G>A	GRCh37
NC_000019.8:g.17144676G>A	NCBI36
NG_013068.1:g.102086G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682292.1:c.2044G>A MANE Select	ENSP00000507803.1:p.Val682Met
ENST00000397274.6:c.2044G>A	ENSP00000380444.2:p.Val682Met
ENST00000594824.5:c.2044G>A	ENSP00000471367.1:p.Val682Met
ENST00000594971.5:c.212G>A
ENST00000595618.5:c.2044G>A	ENSP00000471457.1:p.Val682Met
ENST00000595641.5:c.2044G>A	ENSP00000472915.1:p.Val682Met
ENST00000598101.1:n.55G>A
NM_001130065.1:c.2044G>A	NP_001123537.1:p.Val682Met
NM_004145.3:c.2044G>A	NP_004136.2:p.Val682Met
XM_011528029.1:c.2044G>A	XP_011526331.1:p.Val682Met
XM_011528030.1:c.2044G>A	XP_011526332.1:p.Val682Met
XM_011528031.1:c.2044G>A	XP_011526333.1:p.Val682Met
XM_011528032.1:c.2044G>A	XP_011526334.1:p.Val682Met
XM_011528033.1:c.2044G>A	XP_011526335.1:p.Val682Met
XM_011528034.1:c.2044G>A	XP_011526336.1:p.Val682Met
XM_011528035.1:c.2044G>A	XP_011526337.1:p.Val682Met
XM_011528036.1:c.2044G>A	XP_011526338.1:p.Val682Met
XM_011528037.1:c.2044G>A	XP_011526339.1:p.Val682Met
XM_011528038.1:c.2044G>A	XP_011526340.1:p.Val682Met
XR_936183.1:n.2198G>A
XR_936184.1:n.2198G>A
XR_936185.1:n.2198G>A
NM_001130065.2:c.2044G>A	NP_001123537.1:p.Val682Met
NM_004145.4:c.2044G>A MANE Select	NP_004136.2:p.Val682Met