Canonical Allele Identifier: CA404655644

Gene: MYO9B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.17102533C>G , CM000681.2:g.17102533C>G	GRCh38
NC_000019.9:g.17213343C>G , CM000681.1:g.17213343C>G	GRCh37
NC_000019.8:g.17074343C>G	NCBI36
NG_013068.1:g.31753C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682292.1:c.816C>G MANE Select	ENSP00000507803.1:p.Ile272Met
ENST00000397274.6:c.816C>G	ENSP00000380444.2:p.Ile272Met
ENST00000593411.1:n.352C>G
ENST00000594824.5:c.816C>G	ENSP00000471367.1:p.Ile272Met
ENST00000595618.5:c.816C>G	ENSP00000471457.1:p.Ile272Met
ENST00000595641.5:c.816C>G	ENSP00000472915.1:p.Ile272Met
NM_001130065.1:c.816C>G	NP_001123537.1:p.Ile272Met
NM_004145.3:c.816C>G	NP_004136.2:p.Ile272Met
XM_011528029.1:c.816C>G	XP_011526331.1:p.Ile272Met
XM_011528030.1:c.816C>G	XP_011526332.1:p.Ile272Met
XM_011528031.1:c.816C>G	XP_011526333.1:p.Ile272Met
XM_011528032.1:c.816C>G	XP_011526334.1:p.Ile272Met
XM_011528033.1:c.816C>G	XP_011526335.1:p.Ile272Met
XM_011528034.1:c.816C>G	XP_011526336.1:p.Ile272Met
XM_011528035.1:c.816C>G	XP_011526337.1:p.Ile272Met
XM_011528036.1:c.816C>G	XP_011526338.1:p.Ile272Met
XM_011528037.1:c.816C>G	XP_011526339.1:p.Ile272Met
XM_011528038.1:c.816C>G	XP_011526340.1:p.Ile272Met
XR_936183.1:n.970C>G
XR_936184.1:n.970C>G
XR_936185.1:n.970C>G
NM_001130065.2:c.816C>G	NP_001123537.1:p.Ile272Met
NM_004145.4:c.816C>G MANE Select	NP_004136.2:p.Ile272Met