Canonical Allele Identifier: CA2325729445
Gene: MYO9B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17183487C>G , CM000681.2:g.17183487C>G GRCh38
NC_000019.9:g.17294296C>G , CM000681.1:g.17294296C>G GRCh37
NC_000019.8:g.17155296C>G NCBI36
NG_013068.1:g.112706C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682292.1:c.2334-342C>G MANE Select ENSP00000507803.1:n.2334-342C>G
ENST00000397274.6:c.2334-342C>G ENSP00000380444.2:n.2334-342C>G
ENST00000594824.5:c.2334-342C>G ENSP00000471367.1:n.2334-342C>G
ENST00000594971.5:c.388-342C>G
ENST00000595618.5:c.2334-342C>G ENSP00000471457.1:n.2334-342C>G
ENST00000595641.5:c.2334-342C>G ENSP00000472915.1:n.2334-342C>G
ENST00000598101.1:n.345-342C>G
ENST00000601749.1:n.397-342C>G
ENST00000602177.1:c.210-342C>G ENSP00000472611.1:n.210-342C>G
NM_001130065.1:c.2334-342C>G NP_001123537.1:n.2334-342C>G
NM_004145.3:c.2334-342C>G NP_004136.2:n.2334-342C>G
XM_011528029.1:c.2424-342C>G XP_011526331.1:n.2424-342C>G
XM_011528030.1:c.2424-342C>G XP_011526332.1:n.2424-342C>G
XM_011528031.1:c.2424-342C>G XP_011526333.1:n.2424-342C>G
XM_011528032.1:c.2424-342C>G XP_011526334.1:n.2424-342C>G
XM_011528033.1:c.2334-342C>G XP_011526335.1:n.2334-342C>G
XM_011528034.1:c.2220-342C>G XP_011526336.1:n.2220-342C>G
XM_011528035.1:c.2424-342C>G XP_011526337.1:n.2424-342C>G
XM_011528036.1:c.2424-342C>G XP_011526338.1:n.2424-342C>G
XM_011528037.1:c.2334-342C>G XP_011526339.1:n.2334-342C>G
XM_011528038.1:c.2334-342C>G XP_011526340.1:n.2334-342C>G
XR_936183.1:n.2578-342C>G
XR_936184.1:n.2578-342C>G
XR_936185.1:n.2578-342C>G
NM_001130065.2:c.2334-342C>G NP_001123537.1:n.2334-342C>G
NM_004145.4:c.2334-342C>G MANE Select NP_004136.2:n.2334-342C>G