Canonical Allele Identifier: CA366242901

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522527C>A (hg19) ; chr6:g.157201393C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201393C>A , CM000668.2:g.157201393C>A	GRCh38
NC_000006.11:g.157522527C>A , CM000668.1:g.157522527C>A	GRCh37
NC_000006.10:g.157564219C>A	NCBI36
NG_032093.1:g.428464C>A
NG_032093.2:g.428464C>A
NG_066624.1:g.430368C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5009C>A	ENSP00000055163.8:p.Pro1670His
ENST00000414678.8:c.5078C>A	ENSP00000412835.3:p.Pro1693His
ENST00000637015.2:c.5297C>A	ENSP00000489729.2:p.Pro1766His
ENST00000346085.10:c.5048C>A	ENSP00000344546.5:p.Pro1683His
ENST00000350026.10:c.4760C>A	ENSP00000055163.7:p.Pro1587His
ENST00000414678.7:c.3326C>A	ENSP00000412835.2:p.Pro1109His
ENST00000635849.1:c.2489C>A	ENSP00000490948.1:p.Pro830His
ENST00000635957.1:c.2120C>A	ENSP00000490385.1:p.Pro707His
ENST00000636227.1:n.3631C>A
ENST00000636254.1:n.1088C>A
ENST00000636930.2:c.5168C>A MANE Select	ENSP00000490491.2:p.Pro1723His
ENST00000636940.1:n.3165C>A
ENST00000637015.1:c.2536C>A
ENST00000637568.1:c.2450C>A
ENST00000637741.1:n.1834C>A
ENST00000637810.1:c.2510C>A	ENSP00000489636.1:p.Pro837His
ENST00000637904.1:c.2669C>A	ENSP00000490550.1:p.Pro890His
ENST00000647938.1:c.4799C>A	ENSP00000498155.1:p.Pro1600His
ENST00000346085.9:c.4799C>A	ENSP00000344546.4:p.Pro1600His
ENST00000350026.9:c.4760C>A	ENSP00000055163.7:p.Pro1587His
ENST00000414678.6:c.3326C>A	ENSP00000412835.2:p.Pro1109His
NM_017519.2:c.4760C>A	NP_059989.2:p.Pro1587His
NM_020732.3:c.4799C>A	NP_065783.3:p.Pro1600His
XM_005267069.3:c.4919C>A	XP_005267126.2:p.Pro1640His
XM_011535984.1:c.3998C>A	XP_011534286.1:p.Pro1333His
XM_011535985.1:c.3818C>A	XP_011534287.1:p.Pro1273His
XM_011535986.1:c.3578C>A	XP_011534288.1:p.Pro1193His
XM_011535987.1:c.3197C>A	XP_011534289.1:p.Pro1066His
XM_011535988.1:c.2060C>A	XP_011534290.1:p.Pro687His
NM_001346813.1:c.4919C>A	NP_001333742.1:p.Pro1640His
NM_001363725.1:c.2669C>A	NP_001350654.1:p.Pro890His
XM_011535984.2:c.5129C>A	XP_011534286.2:p.Pro1710His
XM_011535988.3:c.2060C>A	XP_011534290.1:p.Pro687His
XM_017011103.2:c.5030C>A	XP_016866592.1:p.Pro1677His
XM_017011104.1:c.5000C>A	XP_016866593.1:p.Pro1667His
XM_017011105.2:c.4970C>A	XP_016866594.1:p.Pro1657His
XM_017011106.2:c.4841C>A	XP_016866595.1:p.Pro1614His
XM_017011107.2:c.4820C>A	XP_016866596.1:p.Pro1607His
XR_002956289.1:n.5115C>A
NM_001363725.2:c.2669C>A	NP_001350654.1:p.Pro890His
NM_001371656.1:c.5048C>A	NP_001358585.1:p.Pro1683His
NM_001374820.1:c.5048C>A	NP_001361749.1:p.Pro1683His
NM_001374828.1:c.5168C>A MANE Select	NP_001361757.1:p.Pro1723His
NM_017519.3:c.5009C>A	NP_059989.3:p.Pro1670His