Canonical Allele Identifier: CA366242676

Gene: ARID1B

Linked Data

• dbSNP Id: rs1168651010
• MyVariant Identifiers: chr6:g.157522481C>T (hg19) ; chr6:g.157201347C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201347C>T , CM000668.2:g.157201347C>T	GRCh38
NC_000006.11:g.157522481C>T , CM000668.1:g.157522481C>T	GRCh37
NC_000006.10:g.157564173C>T	NCBI36
NG_032093.1:g.428418C>T
NG_032093.2:g.428418C>T
NG_066624.1:g.430322C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4963C>T	ENSP00000055163.8:p.Pro1655Ser
ENST00000414678.8:c.5032C>T	ENSP00000412835.3:p.Pro1678Ser
ENST00000637015.2:c.5251C>T	ENSP00000489729.2:p.Pro1751Ser
ENST00000346085.10:c.5002C>T	ENSP00000344546.5:p.Pro1668Ser
ENST00000350026.10:c.4714C>T	ENSP00000055163.7:p.Pro1572Ser
ENST00000414678.7:c.3280C>T	ENSP00000412835.2:p.Pro1094Ser
ENST00000635849.1:c.2443C>T	ENSP00000490948.1:p.Pro815Ser
ENST00000635957.1:c.2074C>T	ENSP00000490385.1:p.Pro692Ser
ENST00000636227.1:n.3585C>T
ENST00000636254.1:n.1042C>T
ENST00000636930.2:c.5122C>T MANE Select	ENSP00000490491.2:p.Pro1708Ser
ENST00000636940.1:n.3119C>T
ENST00000637015.1:c.2490C>T
ENST00000637568.1:c.2404C>T
ENST00000637741.1:n.1788C>T
ENST00000637810.1:c.2464C>T	ENSP00000489636.1:p.Pro822Ser
ENST00000637904.1:c.2623C>T	ENSP00000490550.1:p.Pro875Ser
ENST00000647938.1:c.4753C>T	ENSP00000498155.1:p.Pro1585Ser
ENST00000346085.9:c.4753C>T	ENSP00000344546.4:p.Pro1585Ser
ENST00000350026.9:c.4714C>T	ENSP00000055163.7:p.Pro1572Ser
ENST00000414678.6:c.3280C>T	ENSP00000412835.2:p.Pro1094Ser
NM_017519.2:c.4714C>T	NP_059989.2:p.Pro1572Ser
NM_020732.3:c.4753C>T	NP_065783.3:p.Pro1585Ser
XM_005267069.3:c.4873C>T	XP_005267126.2:p.Pro1625Ser
XM_011535984.1:c.3952C>T	XP_011534286.1:p.Pro1318Ser
XM_011535985.1:c.3772C>T	XP_011534287.1:p.Pro1258Ser
XM_011535986.1:c.3532C>T	XP_011534288.1:p.Pro1178Ser
XM_011535987.1:c.3151C>T	XP_011534289.1:p.Pro1051Ser
XM_011535988.1:c.2014C>T	XP_011534290.1:p.Pro672Ser
NM_001346813.1:c.4873C>T	NP_001333742.1:p.Pro1625Ser
NM_001363725.1:c.2623C>T	NP_001350654.1:p.Pro875Ser
XM_011535984.2:c.5083C>T	XP_011534286.2:p.Pro1695Ser
XM_011535988.3:c.2014C>T	XP_011534290.1:p.Pro672Ser
XM_017011103.2:c.4984C>T	XP_016866592.1:p.Pro1662Ser
XM_017011104.1:c.4954C>T	XP_016866593.1:p.Pro1652Ser
XM_017011105.2:c.4924C>T	XP_016866594.1:p.Pro1642Ser
XM_017011106.2:c.4795C>T	XP_016866595.1:p.Pro1599Ser
XM_017011107.2:c.4774C>T	XP_016866596.1:p.Pro1592Ser
XR_002956289.1:n.5069C>T
NM_001363725.2:c.2623C>T	NP_001350654.1:p.Pro875Ser
NM_001371656.1:c.5002C>T	NP_001358585.1:p.Pro1668Ser
NM_001374820.1:c.5002C>T	NP_001361749.1:p.Pro1668Ser
NM_001374828.1:c.5122C>T MANE Select	NP_001361757.1:p.Pro1708Ser
NM_017519.3:c.4963C>T	NP_059989.3:p.Pro1655Ser